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: rs11002791
rs11002791
1 10 79040561 intron variant G/A snv 0.37 0.700 1.000 1 2016 2016
dbSNP: rs67372909
rs67372909
1 10 79045259 intron variant T/C snv 0.22 0.700 1.000 1 2019 2019