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: rs4374383
rs4374383
0.776 0.200 2 112013193 intron variant A/G snv 0.58
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis
0.810 1.000 1 2012 2017
dbSNP: rs17174870
rs17174870
1.000 0.080 2 111907624 intron variant C/T snv 0.24
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.800 1.000 1 2011 2011