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: rs2242653
rs2242653
1 1.000 0.120 6 31707988 missense variant G/A snv 0.17 0.15 0.700 1.000 2 2007 2009
dbSNP: rs6916278
rs6916278
1 1.000 0.120 6 31710997 intron variant G/A snv 7.9E-02 0.700 1.000 1 2011 2011
dbSNP: rs9267546
rs9267546
2 0.925 0.160 6 31705659 intron variant G/A snv 0.15 0.700 1.000 1 2009 2009