Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1127354 0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 26
rs7270101 0.776 0.200 20 3213247 intron variant A/C snv 8.7E-02 9.7E-02 10