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: rs193922680
rs193922680
9 0.790 0.080 15 34793398 missense variant C/T snv 4.0E-06 7.0E-06 0.700 0
dbSNP: rs193922681
rs193922681
1 1.000 0.080 15 34794742 missense variant A/G snv 0.700 0
dbSNP: rs1060502823
rs1060502823
1 1.000 0.080 15 34794747 missense variant G/A snv 0.010 1.000 1 2018 2018