0002793

Case	Control
24985	435209

Location	SNP	Gene	Ref>Alt	Alt in Case	Alt in Control	Chi-square	P-value	Odds ratio
chr15:48426484	rs1426654	SLC24A5	A>G	1246	26280	45.0	1.969e-11	0.8216
chr16:80411204	rs79700617	-	C>G	393	9447	39.69	2.97e-10	0.7231
chr15:48392165	rs1834640	-	A>G	1478	30146	36.36	1.639e-09	0.8498
chr19:18820308	rs757318	CRTC1	C>A	25271	452452	34.24	4.883e-09	0.949
chr25:2679949	rs311121	-	G>T	7153	133050	33.82	6.051e-09	0.9269
chr4:128310182	rs6534618	-	G>A	798	17108	33.69	6.469e-09	0.8094
chr13:113979968	rs200506581	GRTP1	C>CCACA	546	12180	32.63	1.117e-08	0.7784
chr10:45243171	rs10900107	-	T>C	1145	23600	32.33	1.299e-08	0.8405
chr2:135911422	Affx-17900027	RAB3GAP1	T>C	12522	228084	31.45	2.048e-08	0.9428
chr3:124307861	rs2651618	KALRN	T>C	589	12915	30.35	3.601e-08	0.7922
chr18:40401519	rs57372542	RIT2	C>T	743	15880	30.25	3.805e-08	0.8126
chr13:113979972	Affx-80297025	GRTP1	A>ACACT	551	12156	29.9	4.557e-08	0.7875
chr19:18829770	rs11668587	CRTC1	A>G	17231	310661	29.66	5.143e-08	0.9494
chr22:23125050	rs12159531	-	C>T	690	14787	28.87	7.751e-08	0.8104
chr4:140631947	rs4863677	MGST2	G>T	954	19799	28.67	8.573e-08	0.8362
chr22:23120695	rs73162949	-	C>T	738	15688	28.65	8.681e-08	0.8165
chr5:106908138	rs163961	EFNA5	A>C	1454	29114	27.88	1.293e-07	0.866
chr25:155053713	rs28884873	-	G>A	8475	140000	27.71	1.412e-07	1.066
chr24:14850341	rs2032598	USP9Y	T>C	127	2685	27.35	1.698e-07	0.6234
chr2:136407479	rs1446585	R3HDM1	A>G	13943	252455	27.2	1.837e-07	0.9485
chr25:154999134	rs6642320	-	G>A	16996	306367	32.96	9.427e-09	0.9449
chr25:155053713	rs28884873	-	G>A	8069	132980	28.98	7.301e-08	1.07
chr15:97945780	rs28435176	-	T>G	1586	24139	27.83	1.323e-07	1.149
chr25:2679949	rs311121	-	G>T	6708	124080	26.34	2.868e-07	0.9332
chr12:94188781	rs73222727	CRADD	T>G	2927	46398	25.78	3.829e-07	1.105
chr12:16958019	rs10846431	-	A>G	18732	336356	25.39	4.683e-07	0.9532
chr4:40204050	rs73808637	RHOH	T>C	831	12103	25.23	5.101e-07	1.199
chr6:126964510	rs4273712	-	A>G	12837	232279	23.87	1.033e-06	0.9499
chr9:7769009	rs2381661	-	A>G	12012	217632	23.73	1.108e-06	0.9489
chr18:28741950	rs17800369	DSC1	A>C	3575	57486	23.42	1.304e-06	1.09
chr20:31340356	rs6141803	-	T>C	8834	146557	23.42	1.301e-06	1.06
chr19:18829770	rs11668587	CRTC1	A>G	16147	290227	22.75	1.846e-06	0.9542
chr25:154986418	rs142918084	-	C>G	1475	29226	22.55	2.048e-06	0.8792
chr2:76413305	rs72822798	-	G>T	8526	155842	22.44	2.165e-06	0.9436
chr2:135911422	Affx-17900027	RAB3GAP1	T>C	10350	188068	22.21	2.445e-06	0.948
chr6:126851160	rs1490384	-	T>C	25442	433596	21.92	2.848e-06	1.044
chr2:135837906	rs7570971	RAB3GAP1	C>A	13552	244334	21.76	3.09e-06	0.9529
chr25:155183483	rs73237015	-	G>A	8832	161110	21.75	3.101e-06	0.9453
chr12:73937446	rs116970416	-	C>T	678	9826	21.72	3.162e-06	1.204
chr3:44004468	rs13081767	-	T>C	11646	210701	21.69	3.204e-06	0.9506

Location

SNP

Gene

Ref>Alt

Alt in Case

Alt in Control

Chi-square

P-value

Odds ratio

chr15:48426484

rs1426654

SLC24A5

A>G

1246

26280

45.0

1.969e-11

0.8216

chr16:80411204

rs79700617

-

C>G

393

9447

39.69

2.97e-10

0.7231

chr15:48392165

rs1834640

-

A>G

1478

30146

36.36

1.639e-09

0.8498

chr19:18820308

rs757318

CRTC1

C>A

25271

452452

34.24

4.883e-09

0.949

chr25:2679949

rs311121

-

G>T

7153

133050

33.82

6.051e-09

0.9269

chr4:128310182

rs6534618

-

G>A

798

17108

33.69

6.469e-09

0.8094

chr13:113979968

rs200506581

GRTP1

C>CCACA

546

12180

32.63

1.117e-08

0.7784

chr10:45243171

rs10900107

-

T>C

1145

23600

32.33

1.299e-08

0.8405

chr2:135911422

Affx-17900027

RAB3GAP1

T>C

12522

228084

31.45

2.048e-08

0.9428

chr3:124307861

rs2651618

KALRN

T>C

589

12915

30.35

3.601e-08

0.7922

chr18:40401519

rs57372542

RIT2

C>T

743

15880

30.25

3.805e-08

0.8126

chr13:113979972

Affx-80297025

GRTP1

A>ACACT

551

12156

29.9

4.557e-08

0.7875

chr19:18829770

rs11668587

CRTC1

A>G

17231

310661

29.66

5.143e-08

0.9494

chr22:23125050

rs12159531

-

C>T

690

14787

28.87

7.751e-08

0.8104

chr4:140631947

rs4863677

MGST2

G>T

954

19799

28.67

8.573e-08

0.8362

chr22:23120695

rs73162949

-

C>T

738

15688

28.65

8.681e-08

0.8165

chr5:106908138

rs163961

EFNA5

A>C

1454

29114

27.88

1.293e-07

0.866

chr25:155053713

rs28884873

-

G>A

8475

140000

27.71

1.412e-07

1.066

chr24:14850341

rs2032598

USP9Y

T>C

127

2685

27.35

1.698e-07

0.6234

chr2:136407479

rs1446585

R3HDM1

A>G

13943

252455

27.2

1.837e-07

0.9485

chr25:154999134

rs6642320

-

G>A

16996

306367

32.96

9.427e-09

0.9449

chr25:155053713

rs28884873

-

G>A

8069

132980

28.98

7.301e-08

1.07

chr15:97945780

rs28435176

-

T>G

1586

24139

27.83

1.323e-07

1.149

chr25:2679949

rs311121

-

G>T

6708

124080

26.34

2.868e-07

0.9332

chr12:94188781

rs73222727

CRADD

T>G

2927

46398

25.78

3.829e-07

1.105

chr12:16958019

rs10846431

-

A>G

18732

336356

25.39

4.683e-07

0.9532

chr4:40204050

rs73808637

RHOH

T>C

831

12103

25.23

5.101e-07

1.199

chr6:126964510

rs4273712

-

A>G

12837

232279

23.87

1.033e-06

0.9499

chr9:7769009

rs2381661

-

A>G

12012

217632

23.73

1.108e-06

0.9489

chr18:28741950

rs17800369

DSC1

A>C

3575

57486

23.42

1.304e-06

1.09

chr20:31340356

rs6141803

-

T>C

8834

146557

23.42

1.301e-06

1.06

chr19:18829770

rs11668587

CRTC1

A>G

16147

290227

22.75

1.846e-06

0.9542

chr25:154986418

rs142918084

-

C>G

1475

29226

22.55

2.048e-06

0.8792

chr2:76413305

rs72822798

-

G>T

8526

155842

22.44

2.165e-06

0.9436

chr2:135911422

Affx-17900027

RAB3GAP1

T>C

10350

188068

22.21

2.445e-06

0.948

chr6:126851160

rs1490384

-

T>C

25442

433596

21.92

2.848e-06

1.044

chr2:135837906

rs7570971

RAB3GAP1

C>A

13552

244334

21.76

3.09e-06

0.9529

chr25:155183483

rs73237015

-

G>A

8832

161110

21.75

3.101e-06

0.9453

chr12:73937446

rs116970416

-

C>T

678

9826

21.72

3.162e-06

1.204

chr3:44004468

rs13081767

-

T>C

11646

210701

21.69

3.204e-06

0.9506

Location	SNP	Gene	Ref>Alt	Alt in Case	Alt in Control	Chi-square	P-value	Odds ratio
chr17:70147870	rs16977110	-	T>C	1201	5449	30.65	3.093e-08	0.8366
chr25:154986418	rs142918084	-	C>G	1587	7026	29.41	5.867e-08	0.8579
chr15:28388274	rs56013620	HERC2	G>A	422	2141	29.29	6.235e-08	0.7494
chr17:9422686	rs12453113	STX8	A>T	9046	36495	28.49	9.412e-08	0.9333
chr20:31340356	rs6141803	-	T>C	9369	33859	25.7	3.99e-07	1.068
chr4:176575077	rs4624612	GPM6A	T>C	1763	7642	24.64	6.915e-07	0.8752
chr25:2679949	rs311121	-	G>T	7153	28980	24.34	8.073e-07	0.9323
chr19:29501786	rs12973370	-	A>G	11446	45659	24.23	8.548e-07	0.9435
chr15:48426484	rs1426654	SLC24A5	A>G	1246	5530	24.08	9.256e-07	0.8559
chr17:72978048	rs113735659	-	T>G	533	2558	23.65	1.158e-06	0.7927
chr10:79785825	rs3758464	POLR3A	T>G	503	2427	23.4	1.319e-06	0.7885
chr16:80411204	rs79700617	-	C>G	393	1955	23.37	1.339e-06	0.7653
chr4:128310182	rs6534618	-	G>A	798	3665	23.16	1.491e-06	0.8276
chr7:98585152	rs219818	TRRAP	G>T	792	3639	23.07	1.56e-06	0.8273
chr1:245532053	rs12091805	KIF26B	T>G	2253	9585	23.0	1.617e-06	0.8916
chr8:125606229	rs4007926	MTSS1	G>A	22546	83639	22.88	1.728e-06	1.048
chr19:18829770	rs11668587	CRTC1	A>G	17231	67887	22.23	2.42e-06	0.9521
chr25:154999134	rs6642320	-	G>A	18225	71710	22.03	2.677e-06	0.9522
chr1:245520118	rs4256853	KIF26B	T>C	1070	4771	21.97	2.771e-06	0.8521
chr14:30973592	rs117749188	-	A>G	1229	4033	21.7	3.188e-06	1.166
chr25:154999134	rs6642320	-	G>A	16996	67223	29.32	6.143e-08	0.9434
chr25:154986418	rs142918084	-	C>G	1475	6538	27.91	1.271e-07	0.8566
chr20:31340356	rs6141803	-	T>C	8834	31904	24.23	8.557e-07	1.068
chr25:155053713	rs28884873	-	G>A	8069	29136	22.44	2.167e-06	1.067
chr19:29501786	rs12973370	-	A>G	10437	41610	22.08	2.616e-06	0.9437
chr17:9422686	rs12453113	STX8	A>T	8301	33264	21.08	4.414e-06	0.9401
chr15:97945780	rs28435176	-	T>G	1586	5310	20.97	4.666e-06	1.142
chr23:24939664	rs146234888	POLA1	C>T	1159	4172	20.93	4.758e-06	1.167
chr4:178019148	rs6846031	-	G>T	24248	90302	20.59	5.683e-06	1.047
chr1:54484482	rs914720	-	C>T	20914	77524	20.41	6.251e-06	1.047
chr25:2685254	rs311142	-	C>T	19937	73897	20.27	6.736e-06	1.047
chr7:9543075	rs2464920	-	A>G	18962	70159	20.12	7.274e-06	1.048
chr20:52771261	rs2762934	CYP24A1	G>A	8504	34009	19.99	7.791e-06	0.9422
chr12:94188781	rs73222727	CRADD	T>G	2927	10180	19.86	8.345e-06	1.101
chr9:5365761	rs968840	PLGRKT	T>A	15540	61370	19.45	1.034e-05	0.9524
chr14:30973592	rs117749188	-	A>G	1201	3966	19.29	1.124e-05	1.157
chr20:31448849	rs6120005	EFCAB8	G>A	8363	30330	19.02	1.291e-05	1.061
chr18:54397622	rs17750015	WDR7	T>C	17812	69853	18.99	1.315e-05	0.9553
chr25:2679949	rs311121	-	G>T	6708	27008	18.96	1.333e-05	0.9381
chr8:129122576	rs2608035	-	G>A	1657	5599	18.95	1.34e-05	1.132

ID	Name	Top Correlation
ICD-10: E079	Disorder of thyroid, unspecified	0/20
ICD-10: E662	Extreme obesity with alveolar hypoventilation	0/20
ICD-10: F410	Panic disorder [episodic paroxysmal anxiety]	0/20
ICD-10: G470	Disorders of initiating and maintaining sleep [insomnias]	0/20
ICD-10: G473	Sleep apnoea	0/20
ICD-10: G478	Other sleep disorders	0/20
ICD-10: G479	Sleep disorder, unspecified	0/20
ICD-10: G500	Trigeminal neuralgia	0/20
ICD-10: H570	Anomalies of pupillary function	0/20
ICD-10: I214	Acute subendocardial myocardial infarction	0/20
ICD-10: I500	Congestive heart failure	0/20
ICD-10: I509	Heart failure, unspecified	0/20
ICD-10: J351	Hypertrophy of tonsils	0/20
ICD-10: J950	Tracheostomy malfunction	0/20
ICD-10: J961	Chronic respiratory failure	0/20
ICD-10: J969	Respiratory failure, unspecified	0/20
ICD-10: J988	Other specified respiratory disorders	0/20
ICD-10: K148	Other diseases of tongue	0/20
ICD-10: K821	Hydrops of gallbladder	0/20
ICD-10: O120	Gestational oedema	0/20
ICD-10: Q892	Congenital malformations of other endocrine glands	0/20
ICD-10: R064	Hyperventilation	0/20
ICD-10: R068	Other and unspecified abnormalities of breathing	0/20
ICD-10: T884	Failed or difficult intubation	0/20

Abnormal pattern of respiration

0002793

Normal Case/Contol ^ⓘ

Sibling Case/Control ^ⓘ

Links

Statistics

Phenotype Definition

Top SNP Information

Associated Diseases ^ⓘ

Abnormal pattern of respiration

0002793

Normal Case/Contol ⓘ

Sibling Case/Control ⓘ

Links

Statistics

Phenotype Definition

Top SNP Information Show Normal Table Show Sibling SNP

Associated Diseases ⓘ Shared SNP diseases No shared SNP diseases

Normal Case/Contol ^ⓘ

Sibling Case/Control ^ⓘ

Top SNP Information

Associated Diseases ^ⓘ