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: rs910050
rs910050
0.925 0.120 6 32347877 intron variant G/C snv 0.42
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2007 2007
dbSNP: rs910050
rs910050
0.925 0.120 6 32347877 intron variant G/C snv 0.42
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009