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: rs10793565
rs10793565
3 10 44892783 intron variant G/C snv 0.53 0.700 1.000 1 2019 2019
dbSNP: rs2281841
rs2281841
3 10 44911160 intron variant T/C snv 0.53 0.700 1.000 1 2016 2016