K40.3

Case	Control
373	459832

Location	SNP	Gene	Ref>Alt	Alt in Case	Alt in Control	Chi-square	P-value	Odds Ratio
chr12:24233322	rs61910038	SOX5	C>T	44	24599	31.01	2.563e-08	2.317
chr2:192441892	rs113513225	-	G>A	32	16191	28.81	8.001e-08	2.548
chr13:22125178	rs73158436	MICU2	C>T	30	15906	24.09	9.176e-07	2.425
chr20:791962	rs79419125	-	G>A	46	28838	23.84	1.047e-06	2.068
chr2:133607065	rs75729721	NCKAP5	A>G	69	49338	23.68	1.138e-06	1.831
chr22:18592189	rs116936371	PEX26	A>C	24	11681	23.59	1.192e-06	2.637
chr1:220381398	rs12132480	RAB3GAP2	A>G	97	76584	23.27	1.41e-06	1.679
chr9:248241	rs16922826	DOCK8	C>T	81	60800	23.23	1.434e-06	1.749
chr1:209108041	rs75852076	-	G>A	50	33000	22.87	1.732e-06	1.987
chr15:97359468	rs78835703	-	G>A	24	11991	22.31	2.319e-06	2.575
chr9:205764	rs10811213	-	C>T	183	167728	22.2	2.461e-06	1.487
chr1:240550225	rs61829207	FMN2	G>T	29	15659	22.17	2.5e-06	2.374
chr1:220229789	rs12734813	-	G>A	89	69652	21.83	2.976e-06	1.684
chr1:82966637	rs112327837	-	T>C	21	9919	21.71	3.169e-06	2.694
chr2:50754090	rs17536438	NRXN1	C>T	55	37740	21.67	3.238e-06	1.898
chr9:9961495	rs10978137	PTPRD	G>T	246	238964	21.56	3.437e-06	1.429
chr6:32592294	rs34411532	-	G>A	168	152344	21.55	3.453e-06	1.495
chr6:32590722	rs17533090	-	G>T	168	152297	21.28	3.966e-06	1.491
chr3:21017751	rs1497506	-	G>A	119	100367	21.18	4.181e-06	1.576
chr4:15302839	rs116623230	-	G>A	39	24098	20.99	4.609e-06	2.089

Location

SNP

Gene

Ref>Alt

Alt in Case

Alt in Control

Chi-square

P-value

Odds Ratio

chr12:24233322

rs61910038

SOX5

C>T

44

24599

31.01

2.563e-08

2.317

chr2:192441892

rs113513225

-

G>A

32

16191

28.81

8.001e-08

2.548

chr13:22125178

rs73158436

MICU2

C>T

30

15906

24.09

9.176e-07

2.425

chr20:791962

rs79419125

-

G>A

46

28838

23.84

1.047e-06

2.068

chr2:133607065

rs75729721

NCKAP5

A>G

69

49338

23.68

1.138e-06

1.831

chr22:18592189

rs116936371

PEX26

A>C

24

11681

23.59

1.192e-06

2.637

chr1:220381398

rs12132480

RAB3GAP2

A>G

97

76584

23.27

1.41e-06

1.679

chr9:248241

rs16922826

DOCK8

C>T

81

60800

23.23

1.434e-06

1.749

chr1:209108041

rs75852076

-

G>A

50

33000

22.87

1.732e-06

1.987

chr15:97359468

rs78835703

-

G>A

24

11991

22.31

2.319e-06

2.575

chr9:205764

rs10811213

-

C>T

183

167728

22.2

2.461e-06

1.487

chr1:240550225

rs61829207

FMN2

G>T

29

15659

22.17

2.5e-06

2.374

chr1:220229789

rs12734813

-

G>A

89

69652

21.83

2.976e-06

1.684

chr1:82966637

rs112327837

-

T>C

21

9919

21.71

3.169e-06

2.694

chr2:50754090

rs17536438

NRXN1

C>T

55

37740

21.67

3.238e-06

1.898

chr9:9961495

rs10978137

PTPRD

G>T

246

238964

21.56

3.437e-06

1.429

chr6:32592294

rs34411532

-

G>A

168

152344

21.55

3.453e-06

1.495

chr6:32590722

rs17533090

-

G>T

168

152297

21.28

3.966e-06

1.491

chr3:21017751

rs1497506

-

G>A

119

100367

21.18

4.181e-06

1.576

chr4:15302839

rs116623230

-

G>A

39

24098

20.99

4.609e-06

2.089

ID	Name	Top Correlation
HP: 0000023	Inguinal hernia	0/20
HP: 0000118	Phenotypic abnormality	0/20
HP: 0003549	Abnormality of connective tissue	0/20
HP: 0004298	Abnormality of the abdominal wall	0/20
HP: 0004299	Hernia of the abdominal wall	0/20
HP: 0010866	Abdominal wall defect	0/20
HP: 0012531	Pain	0/20
HP: 0025031	Abnormality of the digestive system	0/20
HP: 0025142	Constitutional symptom	0/20
HP: 0031520	Groin pain	0/20
HP: 0100541	Femoral hernia	0/20
HP: 0100790	Hernia	0/20

Unilateral or unspecified inguinal hernia, with obstruction, without gangrene

K40.3

Case/Control GWAS ^ⓘ

Links

Statistics

Top SNP Information

Associated Phenotypes ^ⓘ

Unilateral or unspecified inguinal hernia, with obstruction, without gangrene

K40.3

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 ^ⓘ