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: rs1421405659
rs1421405659
13 0.851 0.360 12 101642529 missense variant T/C;G snv 0.700 0
dbSNP: rs564856283
rs564856283
3 12 101642495 missense variant G/A;C snv 3.2E-05 0.700 0