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: rs2139733
rs2139733
3 0.925 0.080 12 117288937 intron variant T/A snv 0.39 0.010 1.000 1 2014 2014
dbSNP: rs2293050
rs2293050
2 0.925 0.080 12 117281017 intron variant C/A;G;T snv 0.010 1.000 1 2014 2014