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: rs3129900
rs3129900
0.882 0.200 6 32338202 intron variant G/T snv 0.83
Chemical and Drug Induced Liver Injury
0.800 1.000 1 2010 2010
dbSNP: rs3129900
rs3129900
0.882 0.200 6 32338202 intron variant G/T snv 0.83
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2010 2010
dbSNP: rs3129900
rs3129900
0.882 0.200 6 32338202 intron variant G/T snv 0.83
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2007 2007