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: rs3197999
rs3197999
6 0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 0.830 1.000 2 2008 2017
dbSNP: rs9822268
rs9822268
2 0.925 0.040 3 49682296 intron variant G/A;T snv 0.700 1.000 1 2007 2007