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: rs1137101
rs1137101
77 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.020 1.000 2 2016 2018
dbSNP: rs1045895
rs1045895
2 0.925 0.080 1 65432298 3 prime UTR variant G/A;T snv 0.010 1.000 1 2016 2016
dbSNP: rs1805092
rs1805092
2 0.925 0.080 1 65570758 missense variant A/G snv 0.010 1.000 1 2016 2016