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: rs121909533
rs121909533
1 1.000 0.080 16 30068824 missense variant A/G snv 0.800 1.000 5 1987 2004
dbSNP: rs121909534
rs121909534
1 1.000 0.080 16 30069384 missense variant G/A snv 0.800 1.000 5 1987 2004
dbSNP: rs138824667
rs138824667
1 1.000 0.080 16 30070156 missense variant G/A;T snv 2.4E-03; 8.0E-06 0.700 1.000 5 1987 2004