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: rs6897932
rs6897932
IL7R
0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.900 0.909 2 2007 2018
dbSNP: rs6897932
rs6897932
IL7R
0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.800 1.000 2 2011 2017
dbSNP: rs3194051
rs3194051
IL7R
0.851 0.200 5 35876172 missense variant A/G snv 0.24 0.28
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.800 1.000 1 2011 2011
dbSNP: rs7717955
rs7717955
IL7R
0.925 0.200 5 35862739 intron variant C/T snv 0.23
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.700 1.000 1 2011 2011