Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17156280 0.925 0.040 7 82414674 intron variant T/C snv 3.4E-02 2
rs1690818 0.925 0.040 11 99625823 intron variant C/T snv 0.61 2
rs62100776
DCC
0.925 0.040 18 53228263 intron variant A/T snv 0.35 2
rs319924
EYS ; PHF3
0.925 0.040 6 63777354 intron variant A/G;T snv 2
rs9825823 0.851 0.080 3 61096480 intron variant T/C snv 0.47 2
rs2017122 0.925 0.040 11 118444134 intron variant C/T snv 4.0E-02 2
rs7973260 0.851 0.120 12 117937681 intron variant A/G snv 0.83 2
rs10884216 0.925 0.040 10 105701367 intergenic variant T/C snv 0.17 2
rs782212 0.925 0.040 1 72479983 intron variant C/T snv 0.34 2
rs2221540 0.925 0.040 11 132846474 intron variant A/G snv 0.11 2
rs111365677 0.925 0.040 1 99463578 upstream gene variant T/C snv 2.3E-03 3
rs112538845 0.925 0.040 4 184084475 downstream gene variant C/T snv 1.7E-02 3
rs11591827 0.925 0.040 10 81128126 intergenic variant G/A snv 8.4E-02 3
rs12555870 0.925 0.040 9 23347726 intron variant A/G snv 0.36 3
rs1411216 0.925 0.040 9 24520196 intergenic variant A/G snv 0.73 3
rs143934587 0.925 0.040 20 19165806 intergenic variant G/A snv 9.1E-03 3
rs1548076 0.925 0.040 15 69934284 intergenic variant G/A snv 0.95 3
rs182377406 0.925 0.040 11 67449378 upstream gene variant A/G snv 4.5E-04 3
rs190783615 0.925 0.040 X 142772620 intergenic variant T/C snv 9.3E-03 3
rs1908557 0.925 0.040 4 89500202 intron variant T/C snv 0.31 3
rs201569130 0.925 0.040 6 1402916 intergenic variant GACA/- delins 1.1E-02 3
rs201921722 0.925 0.040 11 123679999 downstream gene variant -/A delins 9.2E-06 3
rs2979204 0.925 0.040 8 8441347 regulatory region variant T/C snv 0.34 3
rs34102224 0.925 0.040 8 5364506 downstream gene variant G/C snv 0.12 3
rs4761545 0.925 0.040 12 94032692 regulatory region variant G/T snv 0.56 3