Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1541777 2 218722568 intron variant A/G snv 0.51 2
rs1582931 5 123321505 intergenic variant G/A;T snv 2
rs6422513 1 92566910 intron variant G/A;C snv 2
rs6823268 4 145061411 intron variant A/G snv 0.28 2
rs7195386 0.925 0.120 16 24567137 splice region variant T/A;C snv 0.56 2
rs7534091 1 118321993 intergenic variant A/G snv 0.23 2
rs76929617 12 120429995 intergenic variant A/G snv 3.7E-02 2
rs7826312 8 32542597 intron variant T/C snv 0.57 2
rs9880211 3 136388707 intron variant G/A snv 0.19 2