R09.8

Case	Control
275	459930

Location	SNP	Gene	Ref>Alt	Alt in Case	Alt in Control	Chi-square	P-value	Odds Ratio
chr3:89678909	rs115145515	-	G>T	40	30523	27.94	1.25e-07	2.321
chr20:46922625	rs7262846	-	G>A	19	10397	26.62	2.481e-07	3.131
chr16:81948514	rs72824912	PLCG2	A>G	21	12224	26.16	3.143e-07	2.956
chr5:13677225	rs1445688	-	A>G	327	444562	25.81	3.762e-07	1.524
chr5:13695831	rs7724291	DNAH5	T>G	324	441789	24.84	6.214e-07	1.511
chr3:32361733	rs116537770	CMTM8	G>A	28	19556	23.23	1.435e-06	2.468
chr7:28342011	rs78381323	CREB5	A>G	18	10532	22.37	2.247e-06	2.947
chr5:13701536	rs3734110	DNAH5	C>T	315	435270	21.49	3.549e-06	1.47
chr20:13672406	rs117100167	-	T>C	18	10776	21.21	4.107e-06	2.87
chr1:83840174	rs116297572	-	C>T	64	61873	21.13	4.297e-06	1.823
chr4:152758408	rs361202	-	C>T	205	260483	21.08	4.404e-06	1.486
chr2:25720503	rs116431033	DTNB	T>C	42	35952	20.88	4.902e-06	2.049
chr10:106855457	rs56329516	SORCS3	G>A	99	109483	20.79	5.133e-06	1.65
chr3:89747810	rs6781083	-	C>T	45	39197	20.77	5.167e-06	2.001
chr7:142629687	rs4252531	TRPV5	A>G	21	13590	20.75	5.241e-06	2.649
chr22:48826019	rs916268	-	G>A	26	18530	20.5	5.951e-06	2.412
chr12:115749621	rs74868170	-	G>A	20	12712	20.49	5.984e-06	2.691
chr8:24133535	rs17051819	-	G>A	151	181742	20.14	7.198e-06	1.524
chr4:61816336	rs115687960	-	T>C	37	30406	20.1	7.339e-06	2.106
chr18:45085894	rs17798177	-	G>A	44	38427	20.08	7.418e-06	1.992

Location

SNP

Gene

Ref>Alt

Alt in Case

Alt in Control

Chi-square

P-value

Odds Ratio

chr3:89678909

rs115145515

-

G>T

40

30523

27.94

1.25e-07

2.321

chr20:46922625

rs7262846

-

G>A

19

10397

26.62

2.481e-07

3.131

chr16:81948514

rs72824912

PLCG2

A>G

21

12224

26.16

3.143e-07

2.956

chr5:13677225

rs1445688

-

A>G

327

444562

25.81

3.762e-07

1.524

chr5:13695831

rs7724291

DNAH5

T>G

324

441789

24.84

6.214e-07

1.511

chr3:32361733

rs116537770

CMTM8

G>A

28

19556

23.23

1.435e-06

2.468

chr7:28342011

rs78381323

CREB5

A>G

18

10532

22.37

2.247e-06

2.947

chr5:13701536

rs3734110

DNAH5

C>T

315

435270

21.49

3.549e-06

1.47

chr20:13672406

rs117100167

-

T>C

18

10776

21.21

4.107e-06

2.87

chr1:83840174

rs116297572

-

C>T

64

61873

21.13

4.297e-06

1.823

chr4:152758408

rs361202

-

C>T

205

260483

21.08

4.404e-06

1.486

chr2:25720503

rs116431033

DTNB

T>C

42

35952

20.88

4.902e-06

2.049

chr10:106855457

rs56329516

SORCS3

G>A

99

109483

20.79

5.133e-06

1.65

chr3:89747810

rs6781083

-

C>T

45

39197

20.77

5.167e-06

2.001

chr7:142629687

rs4252531

TRPV5

A>G

21

13590

20.75

5.241e-06

2.649

chr22:48826019

rs916268

-

G>A

26

18530

20.5

5.951e-06

2.412

chr12:115749621

rs74868170

-

G>A

20

12712

20.49

5.984e-06

2.691

chr8:24133535

rs17051819

-

G>A

151

181742

20.14

7.198e-06

1.524

chr4:61816336

rs115687960

-

T>C

37

30406

20.1

7.339e-06

2.106

chr18:45085894

rs17798177

-

G>A

44

38427

20.08

7.418e-06

1.992

ID	Name	Top Correlation
HP: 0000118	Phenotypic abnormality	0/20
HP: 0001507	Growth abnormality	0/20
HP: 0001824	Weight loss	0/20
HP: 0002086	Abnormality of the respiratory system	0/20
HP: 0002093	Respiratory insufficiency	0/20
HP: 0002795	Functional respiratory abnormality	0/20
HP: 0002878	Respiratory failure	0/20
HP: 0004323	Abnormality of body weight	0/20
HP: 0004325	Decreased body weight	0/20
HP: 0004326	Cachexia	0/20
HP: 0004395	Malnutrition	0/20
HP: 0011458	Abdominal symptom	0/20
HP: 0025031	Abnormality of the digestive system	0/20
HP: 0025032	Abnormality of digestive system physiology	0/20

Other specified symptoms and signs involving the circulatory and respiratory systems

R09.8

Case/Control GWAS ^ⓘ

Links

Statistics

Top SNP Information

Associated Phenotypes ^ⓘ

Other specified symptoms and signs involving the circulatory and respiratory systems

R09.8

Case/Control GWAS ⓘ

Links

Statistics

Top SNP Information Show Table

Associated Phenotypes ⓘ Shared SNP phenotypes No shared SNP phenotypes

Case/Control GWAS ^ⓘ

Top SNP Information

Associated Phenotypes ^ⓘ