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: rs211037
rs211037
14 0.742 0.240 5 162101274 synonymous variant C/T snv 0.28 0.31 0.010 1.000 1 2014 2014
dbSNP: rs2290732
rs2290732
2 0.925 0.160 5 161897892 3 prime UTR variant A/G;T snv 0.010 1.000 1 2014 2014
dbSNP: rs267606959
rs267606959
19 0.732 0.200 15 89318986 missense variant G/A snv 2.0E-05 0.010 1.000 1 2010 2010