Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs312262717 0.790 0.240 15 44659104 frameshift variant A/-;AA delins 18
rs8321 0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 15
rs1333048 0.683 0.320 9 22125348 intron variant A/C snv 0.44 10
rs11152369 0.851 0.040 18 55399097 intron variant A/C snv 6.3E-02 5
rs1054442
DDN
0.925 0.040 12 48995537 3 prime UTR variant A/C snv 0.46 4
rs17673138 0.851 0.040 8 32840440 intron variant A/C snv 8.6E-02 4
rs137928907 0.882 0.040 12 130827204 missense variant A/C snv 1.4E-02 1.5E-02 3
rs4380187 0.925 0.040 2 184947213 intergenic variant A/C snv 0.34 3
rs182107583 0.925 0.080 2 149675023 intron variant A/C snv 4.2E-03 2
rs7296288
DHH
0.851 0.080 12 49086185 upstream gene variant A/C snv 0.50 2
rs73057489 0.925 0.080 12 17370820 regulatory region variant A/C snv 3.9E-02 2
rs12275195 1.000 0.040 11 79394755 intron variant A/C snv 0.12 1
rs17826395 1.000 0.040 5 7502943 intron variant A/C snv 0.16 1
rs12443954 0.851 0.040 16 89675088 intron variant A/C;G snv 5
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 5
rs28456 0.925 0.120 11 61822009 intron variant A/C;G snv 5
rs2070615 1.000 0.040 12 48824388 intron variant A/C;G snv 4.7E-06; 0.58 1
rs420259 0.925 0.040 16 23622705 intron variant A/C;G snv 1
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 3
rs329319 1.000 0.040 5 134570919 intron variant A/C;G;T snv 1
rs12487445 0.925 0.040 3 52584303 intron variant A/C;T snv 2
rs300774 0.925 0.040 2 112496 intergenic variant A/C;T snv 2
rs11237799 1.000 0.040 11 79356427 intron variant A/C;T snv 1
rs1344706 0.701 0.160 2 184913701 intron variant A/C;T snv 1
rs4447398 1.000 0.040 15 42612706 intron variant A/C;T snv 1