Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11230563
rs11230563
CD6 ; LOC105369326
0.790 0.360 11 61008737 missense variant C/G;T snv 4.2E-06; 0.31
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.800 1.000 2 2012 2015
dbSNP: rs11230563
rs11230563
CD6 ; LOC105369326
0.790 0.360 11 61008737 missense variant C/G;T snv 4.2E-06; 0.31
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.710 1.000 2 2016 2018
dbSNP: rs11230563
rs11230563
CD6 ; LOC105369326
0.790 0.360 11 61008737 missense variant C/G;T snv 4.2E-06; 0.31
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 2 2015 2016
dbSNP: rs11230563
rs11230563
CD6 ; LOC105369326
0.790 0.360 11 61008737 missense variant C/G;T snv 4.2E-06; 0.31
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 2 2015 2016
dbSNP: rs11230563
rs11230563
CD6 ; LOC105369326
0.790 0.360 11 61008737 missense variant C/G;T snv 4.2E-06; 0.31
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
dbSNP: rs11230563
rs11230563
CD6 ; LOC105369326
0.790 0.360 11 61008737 missense variant C/G;T snv 4.2E-06; 0.31
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs11230563
rs11230563
CD6 ; LOC105369326
0.790 0.360 11 61008737 missense variant C/G;T snv 4.2E-06; 0.31
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.010 1.000 1 2013 2013
dbSNP: rs11230563
rs11230563
CD6 ; LOC105369326
0.790 0.360 11 61008737 missense variant C/G;T snv 4.2E-06; 0.31
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.010 1.000 1 2016 2016