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: rs3806265
rs3806265
3 0.882 0.160 1 247423034 intron variant T/C snv 0.41 0.010 1.000 1 2016 2016
dbSNP: rs4612666
rs4612666
10 0.763 0.440 1 247435768 intron variant T/C snv 0.65 0.010 1.000 1 2018 2018