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: rs137852871
rs137852871
2 1.000 0.120 19 41422643 missense variant G/A;C snv 1.2E-05; 4.0E-06 0.700 0
dbSNP: rs137852872
rs137852872
3 0.925 0.120 19 41424496 missense variant T/G snv 0.700 0