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: rs1053338
rs1053338
1 1.000 0.080 3 63982224 missense variant A/G snv 0.14; 1.2E-05 0.10 0.700 1.000 2 2015 2017
dbSNP: rs3821902
rs3821902
1 1.000 0.080 3 63956021 intron variant T/G snv 0.10 0.700 1.000 1 2017 2017