Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2278426 1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 2
rs12979813 19 11232027 intron variant A/G snv 0.30 2
rs737337 0.925 0.040 19 11236817 synonymous variant T/C snv 0.15 0.20 2