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: rs12979860
rs12979860
84 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2016 2016
dbSNP: rs2596538
rs2596538
5 0.851 0.160 6 31400855 intron variant G/A snv 0.41 0.010 1.000 1 2018 2018