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: rs1717027
rs1717027
2 1.000 0.160 3 41946428 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs3774372
rs3774372
3 1.000 0.160 3 41835922 missense variant T/C snv 0.17 0.18 0.700 1.000 1 2011 2011