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: rs121909673
rs121909673
10 0.776 0.080 5 162093965 missense variant G/A snv 0.010 1.000 1 2006 2006
dbSNP: rs211037
rs211037
14 0.742 0.240 5 162101274 synonymous variant C/T snv 0.28 0.31 0.010 1.000 1 2018 2018