Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 30
rs115707823 0.701 0.320 6 30374976 intergenic variant G/A snv 19
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 19
rs1555454508 0.790 0.240 15 44615487 stop gained GTA/ATC mnv 18
rs312262717 0.790 0.240 15 44659104 frameshift variant A/-;AA delins 18
rs12914385 0.790 0.160 15 78606381 intron variant C/A;T snv 13
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 12
rs1057518913 0.851 0.320 9 137762822 splice donor variant T/C snv 7
rs17514846 0.882 0.120 15 90873320 intron variant C/A;G snv 6
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
rs2535629 0.827 0.040 3 52799203 intron variant G/A;C snv 5
rs2721800 0.851 0.040 7 24652933 intron variant G/A;C;T snv 5
rs9297357 0.851 0.040 8 105130105 intron variant C/G;T snv 5
rs9951150 0.851 0.040 18 55153893 intergenic variant A/G;T snv 5
rs11829119 0.851 0.040 12 19040597 intergenic variant T/A;C snv 4
rs141252918 0.882 0.040 6 151506923 intron variant G/A;C snv 4
rs1557136818 0.925 0.120 X 154031259 missense variant C/T snv 4
rs17154917 0.851 0.040 7 81207393 intergenic variant G/A;T snv 4
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 4
rs2054399 0.925 0.040 3 178623794 intron variant G/A;C snv 4
rs221774 0.851 0.080 7 100701361 upstream gene variant A/G;T snv 4
rs2227956 0.752 0.400 6 31810495 missense variant G/A;C;T snv 0.87 4
rs8054556 0.925 0.080 16 29946895 intron variant G/A;C;T snv 4
rs9268856 0.807 0.240 6 32461942 intron variant C/A;T snv 4