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: rs587777601
rs587777601
1 1.000 0.080 22 25207157 missense variant T/A snv 0.800 1.000 2 2005 2013
dbSNP: rs74315490
rs74315490
2 0.925 0.200 22 25207069 missense variant G/A;C snv 2.0E-05; 1.2E-05 0.800 1.000 2 2005 2013