Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs3918226 0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 12
rs13108218 4 3442204 intron variant A/G;T snv 7
rs7740107 1.000 0.080 6 130053316 intron variant T/A;G snv 6
rs1264347 1.000 0.040 6 30830920 upstream gene variant C/T snv 7.9E-02 4
rs34720381 1 171486183 intron variant C/T snv 7.3E-02 4
rs6440003 3 141375367 intron variant G/A snv 0.54 4
rs3795503 1 180936558 synonymous variant C/T snv 0.31 0.27 3
rs6484504 11 31403276 intron variant T/C snv 0.79 3
rs16930370 12 3278531 synonymous variant T/C snv 0.16 0.20 2
rs2267373 22 38204535 intron variant C/T snv 0.58 2
rs41284816 13 50081853 non coding transcript exon variant G/C;T snv 2
rs6544743 2 44163230 upstream gene variant T/A;G snv 2
rs78444298 1 184702964 missense variant G/A snv 1.2E-02 1.2E-02 2