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: rs4648068
rs4648068
9 0.790 0.240 4 102597148 intron variant A/G snv 0.31 0.030 1.000 3 2012 2015
dbSNP: rs28362491
rs28362491
56 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.010 1.000 1 2014 2014
dbSNP: rs3774968
rs3774968
4 0.882 0.120 4 102609955 intron variant A/G snv 0.64 0.010 1.000 1 2014 2014