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: rs3829462
rs3829462
1 1.000 0.040 15 58560880 missense variant C/A;T snv 0.97 0.010 1.000 1 1999 1999
dbSNP: rs6078
rs6078
3 0.882 0.120 15 58541794 missense variant G/A;T snv 7.1E-02; 8.0E-06 0.010 1.000 1 1999 1999