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: rs754466
rs754466
1 10 77920676 intron variant A/G;T snv 0.22 0.800 1.000 1 2011 2011
dbSNP: rs11002319
rs11002319
1 10 77876403 intron variant C/T snv 0.28 0.700 1.000 1 2018 2018
dbSNP: rs1650146
rs1650146
1 10 77928450 non coding transcript exon variant A/G snv 0.72 0.700 1.000 1 2018 2018