Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs143405544 0.925 0.040 5 65459777 intron variant A/G snv 4.8E-03 3
rs143934587 0.925 0.040 20 19165806 intergenic variant G/A snv 9.1E-03 3
rs150175932 1.000 0.040 4 150101495 intron variant T/C snv 1.6E-02 3
rs1548076 0.925 0.040 15 69934284 intergenic variant G/A snv 0.95 3
rs1789891 1.000 0.080 4 99329262 intron variant C/A snv 0.13 3
rs182377406 0.925 0.040 11 67449378 upstream gene variant A/G snv 4.5E-04 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
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
rs1994321 1.000 0.040 11 12065766 upstream gene variant G/T snv 0.33 3
rs200855945 0.925 0.040 12 26124961 5 prime UTR variant ACACGCACAC/-;ACACGCACACACACGCACAC delins 1.6E-02 3
rs201203751 0.925 0.040 5 39203496 intron variant TT/-;T;TTT delins 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
rs2435200 0.925 0.080 17 45994485 intron variant G/A snv 0.40 3
rs34102224 0.925 0.040 8 5364506 downstream gene variant G/C snv 0.12 3
rs34177316 0.925 0.040 4 40985283 intron variant A/-;AA;AAA delins 3
rs34467936 1.000 0.040 11 47893747 intergenic variant A/G snv 0.30 3
rs34668726 1.000 0.040 2 23673031 intron variant C/G snv 0.13 3
rs35825582 1.000 0.040 2 143491193 intron variant G/A snv 0.45 3
rs35863382 1.000 0.040 14 91472532 intron variant C/T snv 6.0E-02 3
rs3843954 1.000 0.040 13 57974377 intergenic variant G/A;C snv 3