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: rs7313422
rs7313422
2 12 20593103 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs9971916
rs9971916
2 12 20535707 intron variant A/T snv 0.99 0.700 1.000 1 2012 2012