Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2710102 0.790 0.120 7 147877298 intron variant A/G;T snv 1
rs352759 0.925 0.040 8 15742205 intron variant T/A snv 3
rs9364726 0.882 0.040 6 164236705 intergenic variant A/G snv 6.5E-02 3
rs112538845 0.925 0.040 4 184084475 downstream gene variant C/T snv 1.7E-02 3
rs1344706 0.701 0.160 2 184913701 intron variant A/C;T snv 1
rs11924809 0.925 0.040 3 186353656 intron variant G/A snv 5.3E-02 3
rs11829119 0.851 0.040 12 19040597 intergenic variant T/A;C snv 4
rs143934587 0.925 0.040 20 19165806 intergenic variant G/A snv 9.1E-03 3
rs10405744 0.851 0.040 19 19948684 intron variant G/A snv 9.0E-02 4
rs6740584 0.882 0.040 2 207564627 intron variant T/C snv 0.37 1
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 7
rs78087832 0.925 0.040 2 224600060 intergenic variant C/T snv 2.4E-03 3
rs12555870 0.925 0.040 9 23347726 intron variant A/G snv 0.36 3
rs6586354 0.851 0.040 1 234897489 intron variant G/A snv 0.25 4
rs2302045 0.851 0.040 2 241081801 splice region variant G/A snv 7.6E-02 1.0E-01 4
rs1411216 0.925 0.040 9 24520196 intergenic variant A/G snv 0.73 3
rs200855945 0.925 0.040 12 26124961 5 prime UTR variant ACACGCACAC/-;ACACGCACACACACGCACAC delins 1.6E-02 3
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs1401635 0.925 0.040 11 27672444 intron variant C/G snv 0.73 2
rs183124483
NLK
0.925 0.040 17 28110028 intron variant G/A snv 7.1E-04 3
rs853679 0.851 0.160 6 28329086 intron variant C/A snv 0.20 4
rs10968749 0.851 0.040 9 28752486 intergenic variant A/G snv 5.5E-02 4
rs9862857 0.851 0.040 3 30453840 regulatory region variant A/G;T snv 4
rs4512342 0.827 0.120 8 32750356 intron variant T/G snv 0.12 1
rs17673138 0.851 0.040 8 32840440 intron variant A/C snv 8.6E-02 4