Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs76064236 1.000 0.080 1 226335330 upstream gene variant T/G snv 2.1E-03 1
rs77138376 1.000 0.080 1 78168337 downstream gene variant G/A;C snv 1
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44
rs5742909 0.614 0.680 2 203867624 upstream gene variant C/T snv 6.7E-02 40
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs4553808 0.672 0.320 2 203866282 upstream gene variant A/G;T snv 0.16 28
rs767830104 0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 13
rs1372834938 0.763 0.280 2 8812465 missense variant G/C snv 4.2E-06 12
rs188942711 0.763 0.200 2 227253336 missense variant G/A;T snv 2.8E-05; 4.0E-06 9
rs16840252 0.776 0.480 2 203866796 upstream gene variant C/T snv 0.16 8
rs121908525 0.790 0.160 2 240875159 missense variant T/C snv 4.4E-05 5.6E-05 7
rs452204 0.807 0.200 2 113131484 intron variant G/A snv 0.45 7
rs13538 1.000 0.080 2 73641201 missense variant A/G snv 0.21 0.31 5
rs7422339 1.000 0.080 2 210675783 missense variant C/A snv 5
rs121908529 0.851 0.160 2 240871433 missense variant G/A;C snv 5.6E-04 4
rs187355703 1.000 0.080 2 176128855 intron variant C/G snv 1.5E-02 1.5E-02 4
rs6431731 1.000 0.080 2 15722878 intron variant C/T snv 0.97 4
rs7588550 0.851 0.160 2 212304043 intron variant G/A snv 0.96 4
rs11123169 1.000 0.080 2 113209498 upstream gene variant C/A;T snv 3
rs11571317 0.882 0.160 2 203867285 upstream gene variant C/T snv 5.2E-02 3
rs3764913 1.000 0.080 2 210210185 non coding transcript exon variant T/C snv 0.30 0.27 3
rs4972593 0.925 0.200 2 173598126 intergenic variant T/A snv 0.20 3