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: rs1566304640
rs1566304640
8 0.827 0.280 13 77900593 missense variant G/A snv 0.700 0
dbSNP: rs781214034
rs781214034
10 0.790 0.320 13 77903538 missense variant C/T snv 1.3E-04 2.8E-05 0.700 0