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: rs1487151044
rs1487151044
5 0.851 0.080 10 31510817 missense variant T/C snv 0.010 1.000 1 2014 2014
dbSNP: rs754854286
rs754854286
3 1.000 0.120 10 31520432 missense variant G/C snv 0.010 1.000 1 2019 2019