0004930

Case	Control
6414	453780

Location	SNP	Gene	Ref>Alt	Alt in Case	Alt in Control	Chi-square	P-value	Odds ratio
chr23:75648551	rs7066146	MAGEE1	A>C	322	16342	36.59	1.46e-09	1.411
chr6:41384515	rs6924912	-	C>T	791	45406	31.71	1.787e-08	1.231
chr4:140811135	rs3733382	MAML3	C>T	3447	221674	30.14	4.018e-08	1.115
chr23:106146349	rs5962774	MORC4	T>C	220	10806	30.08	4.139e-08	1.455
chr2:161430847	rs13427899	-	C>T	452	24487	29.61	5.294e-08	1.299
chr10:117649124	rs7904803	ATRNL1	C>A	350	18336	29.17	6.623e-08	1.342
chr10:114925758	rs1056877	TCF7L2	T>C	246	12205	28.81	7.982e-08	1.415
chr23:64367019	rs7064929	-	G>A	326	17240	28.61	8.838e-08	1.353
chr2:66725070	rs12995572	MEIS1	G>C	485	26666	28.22	1.081e-07	1.28
chr1:44936512	rs6684444	RNF220	A>C	517	28739	27.54	1.539e-07	1.267
chr17:56035019	rs73315832	-	A>C	201	9731	26.96	2.079e-07	1.449
chr1:120451352	rs947273	-	C>A	2184	137670	26.8	2.258e-07	1.129
chr4:37586357	rs4832921	C4orf19	G>A	516	28774	26.8	2.252e-07	1.263
chr23:128909607	rs12007179	-	C>T	347	18703	26.6	2.501e-07	1.327
chr4:190837589	rs6822336	-	C>T	221	10925	26.55	2.567e-07	1.421
chr19:4273631	rs7246722	-	G>A	206	10059	26.37	2.818e-07	1.436
chr16:17680632	rs8044659	-	A>G	259	13158	26.36	2.838e-07	1.382
chr7:12317890	rs72584561	-	A>G	543	30491	26.35	2.845e-07	1.254
chr23:19209307	rs960190	-	T>C	447	25034	25.54	4.335e-07	1.279
chr13:104060087	rs9586179	-	T>C	654	37630	25.49	4.456e-07	1.226
chr6:41384515	rs6924912	-	C>T	776	44597	35.04	3.223e-09	1.247
chr10:125784851	Affx-35292745	CHST15	C>T	3448	261686	23.95	9.869e-07	0.9065
chr10:125789950	rs4929829	CHST15	T>C	3303	250953	23.89	1.021e-06	0.9052
chr9:32679230	rs76755525	-	A>G	315	17161	21.66	3.255e-06	1.306
chr5:171124515	rs10454967	-	C>T	265	14117	21.44	3.646e-06	1.335
chr2:161430847	rs13427899	-	C>T	385	21559	21.32	3.88e-06	1.272
chr10:125780759	Affx-2679766	CHST15	G>C	3282	248798	20.92	4.794e-06	0.911
chr14:73029178	rs2074647	RGS6	G>A	1202	74955	20.68	5.426e-06	1.149
chr16:50781802	rs8060598	CYLD	T>C	5593	377622	20.23	6.862e-06	1.084
chr7:117582736	rs62471815	-	G>A	6093	413311	19.7	9.074e-06	1.082
chr13:33120622	rs12876812	-	C>G	456	39548	19.66	9.228e-06	0.8087
chr5:63294466	rs115426975	-	G>A	318	17651	19.38	1.069e-05	1.286
chr10:77330925	rs34949865	LRMDA	TG>T	3610	239909	19.06	1.27e-05	1.09
chr9:110194198	rs113726944	-	G>A	644	38467	18.95	1.339e-05	1.194
chr10:77344383	rs1430329	LRMDA	C>T	3609	239824	18.93	1.355e-05	1.09
chr2:161413657	rs80082579	-	A>G	382	21655	18.92	1.364e-05	1.255
chr6:22913065	rs1928086	-	T>C	817	49768	18.89	1.388e-05	1.171
chr15:82412578	rs74747638	-	A>C	759	45986	18.88	1.393e-05	1.178
chr4:127181190	rs56243504	-	T>C	631	37669	18.86	1.405e-05	1.196
chr1:188148725	rs1853377	-	C>T	972	78512	18.65	1.571e-05	0.8651

Location

SNP

Gene

Ref>Alt

Alt in Case

Alt in Control

Chi-square

P-value

Odds ratio

chr23:75648551

rs7066146

MAGEE1

A>C

322

16342

36.59

1.46e-09

1.411

chr6:41384515

rs6924912

-

C>T

791

45406

31.71

1.787e-08

1.231

chr4:140811135

rs3733382

MAML3

C>T

3447

221674

30.14

4.018e-08

1.115

chr23:106146349

rs5962774

MORC4

T>C

220

10806

30.08

4.139e-08

1.455

chr2:161430847

rs13427899

-

C>T

452

24487

29.61

5.294e-08

1.299

chr10:117649124

rs7904803

ATRNL1

C>A

350

18336

29.17

6.623e-08

1.342

chr10:114925758

rs1056877

TCF7L2

T>C

246

12205

28.81

7.982e-08

1.415

chr23:64367019

rs7064929

-

G>A

326

17240

28.61

8.838e-08

1.353

chr2:66725070

rs12995572

MEIS1

G>C

485

26666

28.22

1.081e-07

1.28

chr1:44936512

rs6684444

RNF220

A>C

517

28739

27.54

1.539e-07

1.267

chr17:56035019

rs73315832

-

A>C

201

9731

26.96

2.079e-07

1.449

chr1:120451352

rs947273

-

C>A

2184

137670

26.8

2.258e-07

1.129

chr4:37586357

rs4832921

C4orf19

G>A

516

28774

26.8

2.252e-07

1.263

chr23:128909607

rs12007179

-

C>T

347

18703

26.6

2.501e-07

1.327

chr4:190837589

rs6822336

-

C>T

221

10925

26.55

2.567e-07

1.421

chr19:4273631

rs7246722

-

G>A

206

10059

26.37

2.818e-07

1.436

chr16:17680632

rs8044659

-

A>G

259

13158

26.36

2.838e-07

1.382

chr7:12317890

rs72584561

-

A>G

543

30491

26.35

2.845e-07

1.254

chr23:19209307

rs960190

-

T>C

447

25034

25.54

4.335e-07

1.279

chr13:104060087

rs9586179

-

T>C

654

37630

25.49

4.456e-07

1.226

chr6:41384515

rs6924912

-

C>T

776

44597

35.04

3.223e-09

1.247

chr10:125784851

Affx-35292745

CHST15

C>T

3448

261686

23.95

9.869e-07

0.9065

chr10:125789950

rs4929829

CHST15

T>C

3303

250953

23.89

1.021e-06

0.9052

chr9:32679230

rs76755525

-

A>G

315

17161

21.66

3.255e-06

1.306

chr5:171124515

rs10454967

-

C>T

265

14117

21.44

3.646e-06

1.335

chr2:161430847

rs13427899

-

C>T

385

21559

21.32

3.88e-06

1.272

chr10:125780759

Affx-2679766

CHST15

G>C

3282

248798

20.92

4.794e-06

0.911

chr14:73029178

rs2074647

RGS6

G>A

1202

74955

20.68

5.426e-06

1.149

chr16:50781802

rs8060598

CYLD

T>C

5593

377622

20.23

6.862e-06

1.084

chr7:117582736

rs62471815

-

G>A

6093

413311

19.7

9.074e-06

1.082

chr13:33120622

rs12876812

-

C>G

456

39548

19.66

9.228e-06

0.8087

chr5:63294466

rs115426975

-

G>A

318

17651

19.38

1.069e-05

1.286

chr10:77330925

rs34949865

LRMDA

TG>T

3610

239909

19.06

1.27e-05

1.09

chr9:110194198

rs113726944

-

G>A

644

38467

18.95

1.339e-05

1.194

chr10:77344383

rs1430329

LRMDA

C>T

3609

239824

18.93

1.355e-05

1.09

chr2:161413657

rs80082579

-

A>G

382

21655

18.92

1.364e-05

1.255

chr6:22913065

rs1928086

-

T>C

817

49768

18.89

1.388e-05

1.171

chr15:82412578

rs74747638

-

A>C

759

45986

18.88

1.393e-05

1.178

chr4:127181190

rs56243504

-

T>C

631

37669

18.86

1.405e-05

1.196

chr1:188148725

rs1853377

-

C>T

972

78512

18.65

1.571e-05

0.8651

Location	SNP	Gene	Ref>Alt	Alt in Case	Alt in Control	Chi-square	P-value	Odds ratio
chr6:41384515	rs6924912	-	C>T	776	24162	34.84	3.582e-09	1.248
chr9:32679230	rs76755525	-	A>G	315	9222	22.81	1.79e-06	1.318
chr5:171124515	rs10454967	-	C>T	265	7579	22.63	1.968e-06	1.349
chr10:125784851	Affx-35292745	CHST15	C>T	3448	141659	22.59	2.009e-06	0.9086
chr10:125789950	rs4929829	CHST15	T>C	3303	135833	22.22	2.429e-06	0.9079
chr13:33120622	rs12876812	-	C>G	456	21559	20.53	5.871e-06	0.8042
chr2:161430847	rs13427899	-	C>T	385	11740	20.25	6.785e-06	1.266
chr9:110194198	rs113726944	-	G>A	644	20729	20.11	7.317e-06	1.202
chr10:125780759	Affx-2679766	CHST15	G>C	3282	134775	20.07	7.463e-06	0.9123
chr1:188148725	rs1853377	-	C>T	972	42766	19.75	8.827e-06	0.8608
chr14:73029178	rs2074647	RGS6	G>A	1202	40737	19.69	9.128e-06	1.146
chr16:50781802	rs8060598	CYLD	T>C	5593	204822	19.6	9.548e-06	1.083
chr7:117582736	rs62471815	-	G>A	6093	224284	18.83	1.426e-05	1.081
chr7:142497810	rs35750152	-	T>G	5223	209849	18.65	1.571e-05	0.9244
chr6:113970388	rs62417309	-	A>G	1207	40989	18.56	1.65e-05	1.141
chr3:127560006	rs77842558	MGLL	C>T	235	6796	18.46	1.734e-05	1.332
chr4:127181190	rs56243504	-	T>C	631	20450	18.31	1.878e-05	1.194
chr9:85375454	rs4877706	-	G>A	2818	100688	17.82	2.431e-05	1.096
chr2:161413657	rs80082579	-	A>G	382	11802	17.81	2.441e-05	1.249
chr5:63294466	rs115426975	-	G>A	318	9655	17.76	2.5e-05	1.275

ID	Name	Top Correlation
ICD-10: I151	Hypertension secondary to other renal disorders	0/20
ICD-10: I270	Primary pulmonary hypertension	0/20
ICD-10: I272	Other secondary pulmonary hypertension	0/20
ICD-10: I780	Hereditary haemorrhagic telangiectasia	0/20
ICD-10: J984	Other disorders of lung	0/20
ICD-10: M940	Chondrocostal junction syndrome [Tietze]	0/20
ICD-10: O431	Malformation of placenta	0/20
ICD-10: R042	Haemoptysis	0/20

Abnormality of the pulmonary vasculature

0004930

Normal Case/Contol ^ⓘ

Sibling Case/Control ^ⓘ

Links

Statistics

Top SNP Information

Associated Diseases ^ⓘ

Abnormality of the pulmonary vasculature

0004930

Normal Case/Contol ⓘ

Sibling Case/Control ⓘ

Links

Statistics

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 ^ⓘ