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: rs2786098
rs2786098
1 1.000 0.080 1 197356778 intron variant T/A;G snv 0.810 1.000 1 2010 2010