Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs3219090 1.000 0.040 1 226376990 intron variant T/C snv 0.58 1
rs3219125 1.000 0.040 1 226367250 non coding transcript exon variant T/C snv 5.0E-02 1