Source: GWASDB

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: rs17824933
rs17824933
CD6
1.000 0.080 11 60993140 intron variant C/A;G snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.850 1.000 2 2009 2016
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 1 2012 2015
dbSNP: rs4939488
rs4939488
CD6
11 61019002 non coding transcript exon variant T/C;G snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012