Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 7
rs7225002 0.925 0.080 17 46111701 intron variant A/G snv 0.39 7
rs8067056 0.925 0.080 17 46006582 intron variant T/C;G snv 0.30 5
rs9303521 0.925 0.120 17 45727828 intron variant T/C;G snv 0.60 5
rs12938031 0.851 0.160 17 45777136 intron variant A/G snv 0.26 4
rs199505 0.925 0.120 17 46782044 intron variant A/G snv 0.84 4
rs62081501 0.925 0.080 18 37627749 intron variant G/A snv 6.2E-02 4
rs8089865
DCC
1.000 0.040 18 53431552 intron variant G/A;C snv 4
rs10965780 1.000 0.040 9 23341717 intron variant C/G;T snv 3
rs112106319 0.925 0.040 9 115094539 intron variant A/T snv 2.8E-03 3
rs114465512 1.000 0.040 22 22047895 intron variant C/T snv 4.7E-03 3
rs11924809 0.925 0.040 3 186353656 intron variant G/A snv 5.3E-02 3
rs12963463 1.000 0.040 18 55431862 intron variant C/G;T snv 3
rs138472420 1.000 0.040 19 47657765 intron variant G/A snv 3.3E-03 3
rs142484554 0.925 0.040 3 141059454 intron variant GAG/- delins 0.11 3
rs142641502 0.925 0.040 11 33109861 intron variant T/C snv 8.0E-03 3
rs143405544 0.925 0.040 5 65459777 intron variant A/G snv 4.8E-03 3
rs150175932 1.000 0.040 4 150101495 intron variant T/C snv 1.6E-02 3
rs1789891 1.000 0.080 4 99329262 intron variant C/A snv 0.13 3
rs183042538 0.925 0.040 20 41197420 intron variant A/T snv 3.2E-02 3
rs183124483
NLK
0.925 0.040 17 28110028 intron variant G/A snv 7.1E-04 3
rs188843168 0.925 0.040 10 103390184 intron variant T/A;C snv 4.3E-04 3
rs189864513 0.925 0.040 4 52767390 intron variant T/C snv 1.9E-03 3
rs1908557 0.925 0.040 4 89500202 intron variant T/C snv 0.31 3
rs201203751 0.925 0.040 5 39203496 intron variant TT/-;T;TTT delins 3