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: rs4934
rs4934
2 0.925 0.120 14 94614466 missense variant G/A;C snv 0.45 0.010 1.000 1 2000 2000
dbSNP: rs538662666
rs538662666
1 1.000 0.080 14 94614480 synonymous variant G/A snv 5.6E-05 1.4E-05 0.010 1.000 1 2000 2000