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: rs1566967399
rs1566967399
1 15 34792158 missense variant C/T snv 0.700 0
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: rs121912673
rs121912673
4 0.882 0.080 15 34791163 missense variant C/T snv 8.0E-06 2.8E-05 0.010 1.000 1 2015 2015
dbSNP: rs121912677
rs121912677
2 1.000 0.080 15 34793326 missense variant T/C snv 0.010 1.000 1 2015 2015