I45.9

Female Case	Female Control	% Female
73	249790	32%

Male Case	Male Control	% Male
152	210190	68%

Location	SNP	Gene	Ref>Alt	Alt in Case	Alt in Control	Chi-square	P-value	Odds ratio
chr20:10164318	rs78854535	-	C>G	11	7145	39.42	3.425e-10	5.693
chr5:97599553	rs114180399	-	A>G	11	7757	34.98	3.33e-09	5.242
chr5:51233486	rs13182417	-	G>A	19	20067	31.51	1.988e-08	3.621
chr5:98584380	rs80155292	-	G>A	11	8372	30.98	2.613e-08	4.833
chr9:130912857	rs3780836	LCN2	C>T	12	9907	29.97	4.389e-08	4.492
chr13:75128114	rs17718828	-	C>T	32	46195	28.94	7.474e-08	2.787
chr10:95060777	rs79193001	-	T>C	11	8898	28.52	9.266e-08	4.6
chr9:15459821	rs3087653	SNAPC3	A>C	21	25349	27.85	1.308e-07	3.234
chr13:71574642	rs12430521	-	G>A	20	23851	27.29	1.752e-07	3.273
chr20:42825230	rs41282014	OSER1	C>T	8	5397	26.9	2.145e-07	5.368
chr10:10286431	rs77692398	-	T>C	13	12266	26.04	3.346e-07	3.939
chr12:103776489	rs12369026	C12orf42	G>A	53	99018	25.93	3.54e-07	2.321
chr11:59184282	rs79559568	-	G>T	13	12448	25.36	4.756e-07	3.878
chr13:21751164	rs117575190	MRPL57	C>T	9	7092	24.08	9.24e-07	4.632
chr16:81559107	rs117818484	CMIP	T>C	17	19501	23.93	9.989e-07	3.282
chr3:121940661	rs80009321	CASR	G>A	13	12822	23.92	1.002e-06	3.748
chr10:71632205	rs41314992	-	G>A	22	30847	23.63	1.168e-06	2.955
chr4:188284095	rs115949163	-	T>C	9	7215	23.42	1.3e-06	4.55
chr10:10297939	rs7903805	-	C>A	14	14696	23.27	1.405e-06	3.551
chr13:75136407	rs34874826	-	C>A	27	39527	23.01	1.608e-06	2.661

Location	SNP	Gene	Ref>Alt	Alt in Case	Alt in Control	Chi-square	P-value	Odds ratio
chr5:4183436	rs114988791	-	G>A	21	8400	38.19	6.424e-10	3.68
chr6:129269142	rs66972531	LAMA2	A>G	20	8218	34.73	3.789e-09	3.578
chr5:4242256	rs255674	-	T>G	38	22907	30.19	3.915e-08	2.504
chr7:16470464	rs80218505	-	C>T	17	7365	26.71	2.367e-07	3.367
chr3:24604459	rs74441602	-	C>T	13	4833	26.67	2.419e-07	3.887
chr8:144329249	rs117399188	ZFP41	G>A	13	4906	26.03	3.36e-07	3.832
chr18:72231977	rs76009631	CNDP1	C>T	30	17532	25.97	3.467e-07	2.57
chr12:15915361	rs12818846	EPS8	C>T	13	5065	24.67	6.82e-07	3.714
chr5:154715471	rs116472358	-	C>T	21	10582	24.49	7.455e-07	2.907
chr12:16042988	rs118054362	STRAP	C>T	13	5111	24.23	8.527e-07	3.677
chr7:49759582	rs11762195	-	C>G	40	27098	23.54	1.221e-06	2.225
chr16:84083938	rs72799260	-	A>G	13	5339	22.76	1.837e-06	3.549
chr2:158290309	rs16841762	CYTIP	A>C	38	25544	22.7	1.89e-06	2.231
chr18:74698121	rs72987269	MBP	C>T	21	11037	22.64	1.956e-06	2.8
chr21:16756444	rs77682069	-	G>A	21	11041	22.4	2.218e-06	2.785
chr5:99837519	rs116116233	-	G>A	12	4730	22.25	2.389e-06	3.659
chr3:186387243	rs78904050	HRG	T>C	19	9562	22.22	2.426e-06	2.902
chr8:19708448	rs73206584	INTS10	C>A	12	4815	21.81	3.018e-06	3.617
chr4:182571271	rs80184374	-	C>T	18	8945	21.56	3.434e-06	2.931
chr2:136193596	rs116839639	ZRANB3	C>T	14	6138	21.41	3.709e-06	3.3

Location

SNP

Gene

Ref>Alt

Alt in Case

Alt in Control

Chi-square

P-value

Odds ratio

chr5:4183436

rs114988791

-

G>A

21

8400

38.19

6.424e-10

3.68

chr6:129269142

rs66972531

LAMA2

A>G

20

8218

34.73

3.789e-09

3.578

chr5:4242256

rs255674

-

T>G

38

22907

30.19

3.915e-08

2.504

chr7:16470464

rs80218505

-

C>T

17

7365

26.71

2.367e-07

3.367

chr3:24604459

rs74441602

-

C>T

13

4833

26.67

2.419e-07

3.887

chr8:144329249

rs117399188

ZFP41

G>A

13

4906

26.03

3.36e-07

3.832

chr18:72231977

rs76009631

CNDP1

C>T

30

17532

25.97

3.467e-07

2.57

chr12:15915361

rs12818846

EPS8

C>T

13

5065

24.67

6.82e-07

3.714

chr5:154715471

rs116472358

-

C>T

21

10582

24.49

7.455e-07

2.907

chr12:16042988

rs118054362

STRAP

C>T

13

5111

24.23

8.527e-07

3.677

chr7:49759582

rs11762195

-

C>G

40

27098

23.54

1.221e-06

2.225

chr16:84083938

rs72799260

-

A>G

13

5339

22.76

1.837e-06

3.549

chr2:158290309

rs16841762

CYTIP

A>C

38

25544

22.7

1.89e-06

2.231

chr18:74698121

rs72987269

MBP

C>T

21

11037

22.64

1.956e-06

2.8

chr21:16756444

rs77682069

-

G>A

21

11041

22.4

2.218e-06

2.785

chr5:99837519

rs116116233

-

G>A

12

4730

22.25

2.389e-06

3.659

chr3:186387243

rs78904050

HRG

T>C

19

9562

22.22

2.426e-06

2.902

chr8:19708448

rs73206584

INTS10

C>A

12

4815

21.81

3.018e-06

3.617

chr4:182571271

rs80184374

-

C>T

18

8945

21.56

3.434e-06

2.931

chr2:136193596

rs116839639

ZRANB3

C>T

14

6138

21.41

3.709e-06

3.3

ID	Name	Top Correlation
HP: 0000118	Phenotypic abnormality	0/20
HP: 0001626	Abnormality of the cardiovascular system	0/20
HP: 0001678	Atrioventricular block	0/20
HP: 0005150	Abnormal atrioventricular conduction	0/20
HP: 0005172	Left posterior fascicular block	0/20
HP: 0011025	Abnormal cardiovascular system physiology	0/20
HP: 0011705	First degree atrioventricular block	0/20
HP: 0011710	Bundle branch block	0/20
HP: 0011711	Left anterior fascicular block	0/20
HP: 0011712	Right bundle branch block	0/20
HP: 0011713	Left bundle branch block	0/20
HP: 0012722	Heart block	0/20
HP: 0030956	Abnormality of cardiovascular system electrophysiology	0/20
HP: 0031546	Cardiac conduction abnormality	0/20

Conduction disorder, unspecified

I45.9

Female ^ⓘ

Male ^ⓘ

Links

Statistics

Top SNP Information

Associated Phenotypes ^ⓘ

Conduction disorder, unspecified

I45.9

Female ⓘ

Male ⓘ

Links

Statistics

Top SNP Information Show Female Show Male

Associated Phenotypes ⓘ Shared SNP phenotype No shared SNP phenotype

Female ^ⓘ

Male ^ⓘ

Top SNP Information

Associated Phenotypes ^ⓘ