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: rs376103979
rs376103979
3 0.882 0.080 19 29708260 missense variant C/G;T snv 2.8E-05; 1.2E-05 0.010 1.000 1 2013 2013
dbSNP: rs762999184
rs762999184
2 1.000 0.080 22 32478989 missense variant C/A;T snv 4.0E-06 7.0E-06 0.010 1.000 1 2015 2015