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: rs12617656
rs12617656
2 0.925 0.200 2 161994637 intron variant T/C snv 0.35 0.010 1.000 1 2016 2016
dbSNP: rs4664443
rs4664443
1 1.000 0.080 2 162029379 intron variant A/G;T snv 0.010 1.000 1 2016 2016