Source: GWASDB ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1295686
rs1295686
2 0.882 0.160 5 132660151 intron variant T/A;C snv 0.68 0.840 1.000 3 2010 2018