Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1127354 0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 26
rs116855232 0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02 12
rs2228391 0.882 0.160 6 32829996 missense variant T/C snv 1.3E-02 3.9E-03 3
rs185386680 0.925 0.040 6 31207153 downstream gene variant A/G snv 1.2E-03 2
rs1736557 0.925 0.160 1 171110939 missense variant G/A snv 8.2E-02 6.3E-02 2
rs114291795 0.925 0.040 6 31409863 intron variant C/G snv 3.0E-02 2
rs2596487 1.000 0.040 6 31357279 non coding transcript exon variant C/T snv 0.31 1