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: rs62264129
rs62264129
2 3 112352566 intron variant A/T snv 0.27 0.700 1.000 1 2016 2016
dbSNP: rs9868582
rs9868582
1 3 112334080 intron variant G/T snv 0.44 0.700 1.000 1 2019 2019