0000834

Case	Control
8407	451787

Location	SNP	Gene	Ref>Alt	Alt in Case	Alt in Control	Chi-square	P-value	Odds ratio
chr13:106727115	rs117642560	-	T>C	449	31363	31.84	1.677e-08	0.7628
chr7:157567732	rs1622289	PTPRN2	C>G	1979	94778	28.29	1.045e-07	1.137
chr13:104754574	rs9586388	-	T>G	345	14435	21.5	3.533e-06	1.29
chr18:20497459	rs58646517	RBBP8	A>G	2318	113941	20.12	7.282e-06	1.106
chr19:7844922	rs114709773	-	G>A	421	27990	19.67	9.193e-06	0.8025
chr15:93588030	rs1969589	RGMA	C>T	417	27749	19.51	1e-05	0.8024
chr13:106730969	rs75208699	-	C>A	1072	65581	19.32	1.104e-05	0.8698
chr6:70812123	rs7772672	COL19A1	G>A	893	55324	19.28	1.132e-05	0.8591
chr3:15382870	rs2103079	SH3BP5	T>C	3836	193410	19.26	1.143e-05	1.084
chr15:78000321	rs4886521	LINGO1	G>A	8236	458679	19.07	1.26e-05	0.9358
chr13:71009927	rs1930861	-	C>T	4821	273047	19.03	1.287e-05	0.9285
chr21:29448093	rs2831461	-	T>C	588	37678	18.97	1.326e-05	0.8321
chr4:188466109	rs954456	-	C>T	2935	146392	18.54	1.662e-05	1.092
chr13:106722560	rs78484740	-	G>A	1050	64143	18.42	1.769e-05	0.8715
chr16:82314281	rs2317832	-	A>G	1156	54933	18.39	1.798e-05	1.141
chr4:31206742	rs115908840	-	T>C	751	34554	18.21	1.975e-05	1.174
chr2:138060089	rs72852294	THSD7B	C>T	1918	113011	18.19	1.995e-05	0.9013
chr9:19156917	rs72698346	-	C>T	843	39168	18.13	2.058e-05	1.164
chr2:45896437	rs582384	PRKCE	A>C	8531	442664	17.69	2.597e-05	1.066
chr6:87142380	rs62443711	-	G>A	362	15585	17.68	2.613e-05	1.253
chr7:157567732	rs1622289	PTPRN2	C>G	1839	87121	31.74	1.767e-08	1.151
chr13:106727115	rs117642560	-	T>C	438	30419	29.58	5.359e-08	0.7676
chr3:148063638	rs73156112	-	G>A	581	26066	18.96	1.334e-05	1.204
chr19:7844922	rs114709773	-	G>A	410	27214	18.77	1.474e-05	0.8043
chr2:206220293	rs6740963	PARD3B	A>G	4308	245054	18.25	1.936e-05	0.9266
chr18:20497459	rs58646517	RBBP8	A>G	2106	103612	18.14	2.051e-05	1.105
chr16:8901283	rs8046212	PMM2	A>G	828	51431	18.09	2.102e-05	0.8584
chr13:106699522	rs4114406	-	C>T	738	46216	17.96	2.254e-05	0.8516
chr6:87142380	rs62443711	-	G>A	359	15454	17.68	2.62e-05	1.254
chr3:129021795	rs62266910	HMCES	C>T	2537	147357	17.66	2.639e-05	0.9127
chr2:138060089	rs72852294	THSD7B	C>T	1859	109563	17.56	2.788e-05	0.9013
chr6:57313251	rs9475973	PRIM2	G>A	343	23062	17.56	2.781e-05	0.7947
chr12:114039833	rs933872	-	G>T	5077	286343	17.51	2.861e-05	0.9315
chr13:71009927	rs1930861	-	C>T	4528	256466	17.5	2.87e-05	0.9292
chr3:128474	rs115940672	-	G>A	802	37235	17.48	2.908e-05	1.165
chr10:123490869	rs2936874	-	A>C	4585	259262	17.48	2.899e-05	0.9294
chr1:58801118	rs79447694	DAB1	C>T	824	38353	17.44	2.969e-05	1.163
chr11:101972265	rs10791562	-	G>A	7581	393173	17.44	2.967e-05	1.068
chr5:114682226	rs76586838	-	G>C	669	30623	17.42	3.004e-05	1.181
chr1:74675210	rs12754465	FPGT	T>C	552	24860	17.4	3.026e-05	1.2

Location

SNP

Gene

Ref>Alt

Alt in Case

Alt in Control

Chi-square

P-value

Odds ratio

chr13:106727115

rs117642560

-

T>C

449

31363

31.84

1.677e-08

0.7628

chr7:157567732

rs1622289

PTPRN2

C>G

1979

94778

28.29

1.045e-07

1.137

chr13:104754574

rs9586388

-

T>G

345

14435

21.5

3.533e-06

1.29

chr18:20497459

rs58646517

RBBP8

A>G

2318

113941

20.12

7.282e-06

1.106

chr19:7844922

rs114709773

-

G>A

421

27990

19.67

9.193e-06

0.8025

chr15:93588030

rs1969589

RGMA

C>T

417

27749

19.51

1e-05

0.8024

chr13:106730969

rs75208699

-

C>A

1072

65581

19.32

1.104e-05

0.8698

chr6:70812123

rs7772672

COL19A1

G>A

893

55324

19.28

1.132e-05

0.8591

chr3:15382870

rs2103079

SH3BP5

T>C

3836

193410

19.26

1.143e-05

1.084

chr15:78000321

rs4886521

LINGO1

G>A

8236

458679

19.07

1.26e-05

0.9358

chr13:71009927

rs1930861

-

C>T

4821

273047

19.03

1.287e-05

0.9285

chr21:29448093

rs2831461

-

T>C

588

37678

18.97

1.326e-05

0.8321

chr4:188466109

rs954456

-

C>T

2935

146392

18.54

1.662e-05

1.092

chr13:106722560

rs78484740

-

G>A

1050

64143

18.42

1.769e-05

0.8715

chr16:82314281

rs2317832

-

A>G

1156

54933

18.39

1.798e-05

1.141

chr4:31206742

rs115908840

-

T>C

751

34554

18.21

1.975e-05

1.174

chr2:138060089

rs72852294

THSD7B

C>T

1918

113011

18.19

1.995e-05

0.9013

chr9:19156917

rs72698346

-

C>T

843

39168

18.13

2.058e-05

1.164

chr2:45896437

rs582384

PRKCE

A>C

8531

442664

17.69

2.597e-05

1.066

chr6:87142380

rs62443711

-

G>A

362

15585

17.68

2.613e-05

1.253

chr7:157567732

rs1622289

PTPRN2

C>G

1839

87121

31.74

1.767e-08

1.151

chr13:106727115

rs117642560

-

T>C

438

30419

29.58

5.359e-08

0.7676

chr3:148063638

rs73156112

-

G>A

581

26066

18.96

1.334e-05

1.204

chr19:7844922

rs114709773

-

G>A

410

27214

18.77

1.474e-05

0.8043

chr2:206220293

rs6740963

PARD3B

A>G

4308

245054

18.25

1.936e-05

0.9266

chr18:20497459

rs58646517

RBBP8

A>G

2106

103612

18.14

2.051e-05

1.105

chr16:8901283

rs8046212

PMM2

A>G

828

51431

18.09

2.102e-05

0.8584

chr13:106699522

rs4114406

-

C>T

738

46216

17.96

2.254e-05

0.8516

chr6:87142380

rs62443711

-

G>A

359

15454

17.68

2.62e-05

1.254

chr3:129021795

rs62266910

HMCES

C>T

2537

147357

17.66

2.639e-05

0.9127

chr2:138060089

rs72852294

THSD7B

C>T

1859

109563

17.56

2.788e-05

0.9013

chr6:57313251

rs9475973

PRIM2

G>A

343

23062

17.56

2.781e-05

0.7947

chr12:114039833

rs933872

-

G>T

5077

286343

17.51

2.861e-05

0.9315

chr13:71009927

rs1930861

-

C>T

4528

256466

17.5

2.87e-05

0.9292

chr3:128474

rs115940672

-

G>A

802

37235

17.48

2.908e-05

1.165

chr10:123490869

rs2936874

-

A>C

4585

259262

17.48

2.899e-05

0.9294

chr1:58801118

rs79447694

DAB1

C>T

824

38353

17.44

2.969e-05

1.163

chr11:101972265

rs10791562

-

G>A

7581

393173

17.44

2.967e-05

1.068

chr5:114682226

rs76586838

-

G>C

669

30623

17.42

3.004e-05

1.181

chr1:74675210

rs12754465

FPGT

T>C

552

24860

17.4

3.026e-05

1.2

Location	SNP	Gene	Ref>Alt	Alt in Case	Alt in Control	Chi-square	P-value	Odds ratio
chr7:157567732	rs1622289	PTPRN2	C>G	1839	38144	32.56	1.155e-08	1.155
chr13:106727115	rs117642560	-	T>C	438	13266	27.38	1.675e-07	0.7735
chr18:20497459	rs58646517	RBBP8	A>G	2106	45156	21.06	4.455e-06	1.116
chr6:89969019	rs73752715	GABRR2	T>C	3105	68029	19.72	8.961e-06	1.094
chr3:148063638	rs73156112	-	G>A	581	11408	19.24	1.15e-05	1.209
chr3:128474	rs115940672	-	G>A	802	16238	18.77	1.472e-05	1.174
chr21:22689344	rs11088859	NCAM2	G>A	310	5706	18.52	1.684e-05	1.287
chr6:57313251	rs9475973	PRIM2	G>A	343	10202	18.26	1.93e-05	0.7894
chr5:114682226	rs76586838	-	G>C	669	13390	17.97	2.248e-05	1.187
chr18:24908364	rs72888039	-	C>T	2003	43140	17.97	2.247e-05	1.109
chr6:57288764	rs9475938	PRIM2	T>C	341	10108	17.52	2.847e-05	0.7927
chr3:129035031	rs14323	H1-10	C>T	1896	49022	17.37	3.082e-05	0.9016
chr1:153978832	rs76014503	NUP210L	C>T	875	17941	17.36	3.088e-05	1.16
chr6:87142380	rs62443711	-	G>A	359	6788	17.22	3.331e-05	1.254
chr18:20582701	rs62095234	RBBP8	C>G	2069	44753	17.17	3.41e-05	1.105
chr2:138060089	rs72852294	THSD7B	C>T	1859	48128	17.14	3.469e-05	0.9014
chr3:66525302	rs4345018	LRIG1	T>C	2283	58497	17.06	3.63e-05	0.9096
chr3:128728502	rs55828563	EFCC1	C>T	1255	33174	16.84	4.073e-05	0.8846
chr11:101972265	rs10791562	-	G>A	7581	172768	16.78	4.2e-05	1.067
chr5:78842918	rs75926313	-	C>T	519	14661	16.74	4.29e-05	0.8308

ID	Name	Top Correlation
ICD-10: C160	Cardia	0/20
ICD-10: C786	Secondary malignant neoplasm of retroperitoneum and peritoneum	0/20
ICD-10: C797	Secondary malignant neoplasm of adrenal gland	0/20
ICD-10: D350	Adrenal gland	0/20
ICD-10: E249	Cushing's syndrome, unspecified	0/20
ICD-10: E260	Primary hyperaldosteronism	0/20
ICD-10: E271	Primary adrenocortical insufficiency	0/20
ICD-10: E274	Other and unspecified adrenocortical insufficiency	0/20
ICD-10: E279	Disorder of adrenal gland, unspecified	0/20
ICD-10: E875	Hyperkalaemia	0/20
ICD-10: E876	Hypokalaemia	0/20
ICD-10: K510	Ulcerative (chronic) enterocolitis	0/20
ICD-10: N489	Disorder of penis, unspecified	0/20
ICD-10: O679	Intrapartum haemorrhage, unspecified	0/20
ICD-10: R935	Abnormal findings on diagnostic imaging of other abdominal regions, including retroperitoneum	0/20

Abnormality of the adrenal glands

0000834

Normal Case/Contol ^ⓘ

Sibling Case/Control ^ⓘ

Links

Statistics

Phenotype Definition

Top SNP Information

Associated Diseases ^ⓘ

Abnormality of the adrenal glands

0000834

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 ^ⓘ