Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7069750
FAS
0.807 0.120 10 89002619 non coding transcript exon variant G/C;T snv 0.50 6
rs7127214 0.807 0.120 11 36322143 intron variant C/G;T snv 6
rs72698115 0.807 0.120 1 154406893 intron variant A/C snv 7.2E-02 6
rs73300638 0.807 0.120 7 28147725 intron variant A/C;G snv 6
rs7909519 0.807 0.120 10 6047878 intron variant T/G snv 7.2E-02 6
rs79893749 0.807 0.120 3 46212159 intron variant C/T snv 0.10 6