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: rs13019832
rs13019832
3 2 60483436 intron variant G/A snv 0.39 0.700 1.000 1 2009 2009
dbSNP: rs2665668
rs2665668
1 2 60541843 3 prime UTR variant G/A snv 0.62 0.58 0.700 1.000 1 2019 2019
dbSNP: rs6731647
rs6731647
1 2 60477604 intron variant T/A;C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs7606173
rs7606173
5 1.000 0.080 2 60498316 intron variant G/C;T snv 0.39 0.700 1.000 1 2009 2009