0100537

Case	Control
12045	448149

Location	SNP	Gene	Ref>Alt	Alt in Case	Alt in Control	Chi-square	P-value	Odds ratio
chr15:48426484	rs1426654	SLC24A5	A>G	461	27065	93.16	4.833e-22	0.6353
chr20:2315543	rs6132532	AL121899.2	A>G	1015	48519	59.63	1.145e-14	0.7793
chr15:48392165	rs1834640	-	A>G	606	31018	58.2	2.373e-14	0.7295
chr6:170242949	rs9396958	-	T>C	268	15846	55.26	1.058e-13	0.6336
chr5:106908138	rs163961	EFNA5	A>C	616	29952	41.3	1.305e-10	0.7678
chr6:163664217	rs16894688	PACRG	A>G	221	12664	39.29	3.649e-10	0.6544
chr6:3185712	rs7754077	-	C>T	349	18323	38.86	4.561e-10	0.7135
chr5:147863034	rs9325101	HTR4	A>G	306	16434	38.82	4.651e-10	0.6978
chr10:49805216	rs11101394	ARHGAP22	C>T	342	18015	38.65	5.077e-10	0.7117
chr5:33951693	rs16891982	SLC45A2	G>C	1487	65571	38.64	5.103e-10	0.8455
chr3:122328753	rs2173764	PARP15	A>G	249	13870	38.52	5.431e-10	0.6729
chr12:56755058	rs4301822	APOF	A>G	216	12396	38.47	5.568e-10	0.6542
chr15:45491394	rs1648299	SHF	T>C	318	16841	37.25	1.037e-09	0.7075
chr2:211717706	rs12995612	-	C>G	303	16169	37.14	1.102e-09	0.7021
chr15:47388375	rs55766414	-	G>A	319	16853	36.74	1.35e-09	0.7096
chr5:54280007	rs1508890	ESM1	C>A	347	18069	36.67	1.402e-09	0.7196
chr6:170602429	rs17860704	DLL1	T>C	200	11518	36.35	1.65e-09	0.6515
chr14:96192566	rs58701215	-	G>C	458	22828	36.27	1.717e-09	0.7513
chr15:73142636	rs4777559	-	C>T	272	14714	36.02	1.954e-09	0.6927
chr19:42393286	rs717225	ARHGEF1	A>G	428	21515	35.91	2.064e-09	0.7453
chr2:38009280	rs13404698	-	A>G	2765	112638	25.68	4.039e-07	0.9015
chr14:45194762	rs229748	-	A>G	7896	307717	25.25	5.047e-07	0.9325
chr6:25918225	rs80215559	SLC17A2	T>C	2022	67673	23.7	1.123e-06	1.122
chr1:11633667	rs12141055	-	C>T	2686	91446	22.75	1.848e-06	1.104
chr5:127347013	rs34145453	-	A>G	9180	328028	22.71	1.883e-06	1.066
chr3:43201732	rs77127731	-	A>G	905	28774	22.56	2.033e-06	1.177
chr8:8569724	rs883647	-	G>A	8924	345411	22.51	2.092e-06	0.9378
chr5:127548955	rs36694	-	A>C	6522	230486	22.03	2.685e-06	1.071
chr2:38009156	rs7568782	-	A>G	3430	137419	21.35	3.834e-06	0.9174
chr1:9338689	rs10746487	-	C>T	6290	245811	20.96	4.686e-06	0.9342
chr6:32050758	rs1150754	TNXB	C>T	4385	153109	20.63	5.562e-06	1.08
chr6:25842951	rs1408272	SLC17A3	T>G	2068	69816	20.62	5.591e-06	1.112
chr1:11595293	rs2235661	DISP3	A>G	3523	121979	20.6	5.645e-06	1.088
chr8:9981854	rs17689674	MSRA	C>A	11128	400763	20.45	6.113e-06	1.061
chr6:32028149	rs1150758	TNXB	G>C	4378	153004	20.32	6.543e-06	1.079
chr5:8350701	rs2136166	-	G>A	8419	324973	20.26	6.749e-06	0.939
chr6:26285683	rs2393593	H4C8	C>T	11610	418950	19.92	8.082e-06	1.06
chr2:8193596	rs72779104	-	G>A	3044	104845	19.9	8.162e-06	1.092
chr9:3248543	rs636548	RFX3	T>G	3140	108332	19.78	8.687e-06	1.09
chr5:127552590	rs2546147	-	A>G	6532	231676	19.77	8.73e-06	1.068

Location

SNP

Gene

Ref>Alt

Alt in Case

Alt in Control

Chi-square

P-value

Odds ratio

chr15:48426484

rs1426654

SLC24A5

A>G

461

27065

93.16

4.833e-22

0.6353

chr20:2315543

rs6132532

AL121899.2

A>G

1015

48519

59.63

1.145e-14

0.7793

chr15:48392165

rs1834640

-

A>G

606

31018

58.2

2.373e-14

0.7295

chr6:170242949

rs9396958

-

T>C

268

15846

55.26

1.058e-13

0.6336

chr5:106908138

rs163961

EFNA5

A>C

616

29952

41.3

1.305e-10

0.7678

chr6:163664217

rs16894688

PACRG

A>G

221

12664

39.29

3.649e-10

0.6544

chr6:3185712

rs7754077

-

C>T

349

18323

38.86

4.561e-10

0.7135

chr5:147863034

rs9325101

HTR4

A>G

306

16434

38.82

4.651e-10

0.6978

chr10:49805216

rs11101394

ARHGAP22

C>T

342

18015

38.65

5.077e-10

0.7117

chr5:33951693

rs16891982

SLC45A2

G>C

1487

65571

38.64

5.103e-10

0.8455

chr3:122328753

rs2173764

PARP15

A>G

249

13870

38.52

5.431e-10

0.6729

chr12:56755058

rs4301822

APOF

A>G

216

12396

38.47

5.568e-10

0.6542

chr15:45491394

rs1648299

SHF

T>C

318

16841

37.25

1.037e-09

0.7075

chr2:211717706

rs12995612

-

C>G

303

16169

37.14

1.102e-09

0.7021

chr15:47388375

rs55766414

-

G>A

319

16853

36.74

1.35e-09

0.7096

chr5:54280007

rs1508890

ESM1

C>A

347

18069

36.67

1.402e-09

0.7196

chr6:170602429

rs17860704

DLL1

T>C

200

11518

36.35

1.65e-09

0.6515

chr14:96192566

rs58701215

-

G>C

458

22828

36.27

1.717e-09

0.7513

chr15:73142636

rs4777559

-

C>T

272

14714

36.02

1.954e-09

0.6927

chr19:42393286

rs717225

ARHGEF1

A>G

428

21515

35.91

2.064e-09

0.7453

chr2:38009280

rs13404698

-

A>G

2765

112638

25.68

4.039e-07

0.9015

chr14:45194762

rs229748

-

A>G

7896

307717

25.25

5.047e-07

0.9325

chr6:25918225

rs80215559

SLC17A2

T>C

2022

67673

23.7

1.123e-06

1.122

chr1:11633667

rs12141055

-

C>T

2686

91446

22.75

1.848e-06

1.104

chr5:127347013

rs34145453

-

A>G

9180

328028

22.71

1.883e-06

1.066

chr3:43201732

rs77127731

-

A>G

905

28774

22.56

2.033e-06

1.177

chr8:8569724

rs883647

-

G>A

8924

345411

22.51

2.092e-06

0.9378

chr5:127548955

rs36694

-

A>C

6522

230486

22.03

2.685e-06

1.071

chr2:38009156

rs7568782

-

A>G

3430

137419

21.35

3.834e-06

0.9174

chr1:9338689

rs10746487

-

C>T

6290

245811

20.96

4.686e-06

0.9342

chr6:32050758

rs1150754

TNXB

C>T

4385

153109

20.63

5.562e-06

1.08

chr6:25842951

rs1408272

SLC17A3

T>G

2068

69816

20.62

5.591e-06

1.112

chr1:11595293

rs2235661

DISP3

A>G

3523

121979

20.6

5.645e-06

1.088

chr8:9981854

rs17689674

MSRA

C>A

11128

400763

20.45

6.113e-06

1.061

chr6:32028149

rs1150758

TNXB

G>C

4378

153004

20.32

6.543e-06

1.079

chr5:8350701

rs2136166

-

G>A

8419

324973

20.26

6.749e-06

0.939

chr6:26285683

rs2393593

H4C8

C>T

11610

418950

19.92

8.082e-06

1.06

chr2:8193596

rs72779104

-

G>A

3044

104845

19.9

8.162e-06

1.092

chr9:3248543

rs636548

RFX3

T>G

3140

108332

19.78

8.687e-06

1.09

chr5:127552590

rs2546147

-

A>G

6532

231676

19.77

8.73e-06

1.068

Location	SNP	Gene	Ref>Alt	Alt in Case	Alt in Control	Chi-square	P-value	Odds ratio
chr15:48426484	rs1426654	SLC24A5	A>G	461	11267	64.37	1.029e-15	0.6821
chr20:2315543	rs6132532	AL121899.2	A>G	1015	21041	44.94	2.035e-11	0.8029
chr15:48392165	rs1834640	-	A>G	606	13074	37.46	9.342e-10	0.7735
chr6:170242949	rs9396958	-	T>C	268	6516	35.98	1.995e-09	0.6882
chr6:163664217	rs16894688	PACRG	A>G	221	5475	32.8	1.02e-08	0.6756
chr14:96192566	rs58701215	-	G>C	458	10078	32.78	1.034e-08	0.7594
chr12:56755058	rs4301822	APOF	A>G	216	5325	31.03	2.535e-08	0.6798
chr10:49805216	rs11101394	ARHGAP22	C>T	342	7770	30.35	3.603e-08	0.7368
chr3:122328753	rs2173764	PARP15	A>G	249	5924	29.61	5.289e-08	0.7033
chr5:106908138	rs163961	EFNA5	A>C	616	12856	28.93	7.502e-08	0.7991
chr6:3185712	rs7754077	-	C>T	349	7816	28.28	1.049e-07	0.7468
chr2:36969753	rs11689624	VIT	G>C	2787	51629	28.25	1.067e-07	0.8962
chr12:29785825	rs11050328	TMTC1	A>C	1545	29669	28.11	1.147e-07	0.867
chr15:45491394	rs1648299	SHF	T>C	318	7181	27.25	1.79e-07	0.7409
chr15:47388375	rs55766414	-	G>A	319	7197	27.08	1.954e-07	0.7419
chr12:56722060	rs1918496	PAN2	G>T	203	4934	27.06	1.976e-07	0.6894
chr6:37145523	rs10223418	-	G>T	201	4885	26.9	2.139e-07	0.6889
chr5:147863034	rs9325101	HTR4	A>G	306	6907	26.08	3.268e-07	0.7415
chr15:73142636	rs4777559	-	C>T	272	6238	25.85	3.689e-07	0.7295
chr1:204438643	rs1553921	PIK3C2B	T>G	624	12868	25.81	3.768e-07	0.8102
chr2:38009280	rs13404698	-	A>G	2765	50196	23.71	1.121e-06	0.9038
chr14:45194762	rs229748	-	A>G	7896	137327	23.52	1.233e-06	0.9338
chr8:8569724	rs883647	-	G>A	8924	154307	22.07	2.634e-06	0.9375
chr3:43201732	rs77127731	-	A>G	905	12848	21.79	3.045e-06	1.178
chr5:127347013	rs34145453	-	A>G	9180	146563	21.52	3.502e-06	1.066
chr5:8350701	rs2136166	-	G>A	8419	145530	21.45	3.623e-06	0.9363
chr2:38009156	rs7568782	-	A>G	3430	61287	19.93	8.047e-06	0.9189
chr1:11633667	rs12141055	-	C>T	2686	41016	19.89	8.221e-06	1.099
chr2:100670107	rs11691359	AFF3	C>T	4299	66947	19.64	9.369e-06	1.08
chr18:36945085	rs9962046	-	T>C	2775	42474	19.36	1.083e-05	1.096
chr8:11831948	rs7461062	DEFB136	C>T	11332	194020	19.2	1.179e-05	0.9434
chr11:96046947	rs78482221	MAML2	A>G	617	12231	18.85	1.413e-05	0.8342
chr8:9981854	rs17689674	MSRA	C>A	11128	179185	18.34	1.848e-05	1.059
chr1:84948165	rs6684882	RPF1	A>G	2500	38226	18.33	1.857e-05	1.098
chr8:840094	rs77263188	DLGAP2	A>G	272	5875	18.25	1.934e-05	0.7666
chr6:29324599	rs10484546	OR5V1	A>C	3034	54073	18.13	2.058e-05	0.9183
chr5:7316956	rs11750162	-	A>G	6307	109830	18.11	2.09e-05	0.9378
chr13:108157360	rs78056606	FAM155A	T>C	1398	20732	17.95	2.265e-05	1.128
chr5:127548955	rs36694	-	A>C	6522	103393	17.82	2.434e-05	1.065
chr14:79218828	rs76995606	NRXN3	C>G	779	11093	17.82	2.427e-05	1.172

ID	Name	Top Correlation
ICD: D892	Hypergammaglobulinaemia, unspecified	1/20
ICD: L031	Cellulitis of other parts of limb	10/20

ID	Name	Top Correlation
ICD-10: A46	Erysipelas	0/20
ICD-10: A491	Streptococcal infection, unspecified	0/20
ICD-10: H601	Cellulitis of external ear	0/20
ICD-10: L030	Cellulitis of finger and toe	0/20
ICD-10: L033	Cellulitis of trunk	0/20
ICD-10: L038	Cellulitis of other sites	0/20
ICD-10: L039	Cellulitis, unspecified	0/20
ICD-10: M722	Plantar fascial fibromatosis	0/20
ICD-10: M766	Achilles tendinitis	0/20
ICD-10: M771	Lateral epicondylitis	0/20
ICD-10: M775	Other enthesopathy of foot	0/20
ICD-10: N764	Abscess of vulva	0/20

Fasciitis

0100537

Normal Case/Contol ^ⓘ

Sibling Case/Control ^ⓘ

Links

Statistics

Phenotype Definition

Top SNP Information

Associated Diseases ^ⓘ

Fasciitis

0100537

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 ^ⓘ