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: rs11797
rs11797
2 0.925 0.160 3 48467186 synonymous variant T/C snv 0.63 0.010 1.000 1 2019 2019
dbSNP: rs61756766
rs61756766
9 0.776 0.320 22 41925447 missense variant G/A snv 5.7E-03 5.7E-03 0.010 1.000 1 2015 2015