Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1994321 1.000 0.040 11 12065766 upstream gene variant G/T snv 0.33 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
rs34102224 0.925 0.040 8 5364506 downstream gene variant G/C snv 0.12 3
rs34467936 1.000 0.040 11 47893747 intergenic variant A/G snv 0.30 3
rs3843954 1.000 0.040 13 57974377 intergenic variant G/A;C snv 3
rs56388524 0.925 0.040 5 45757459 intergenic variant C/A;T snv 2.0E-02 3
rs61572747 1.000 0.040 17 45383525 regulatory region variant A/G snv 0.25 3
rs6546604 0.925 0.040 2 70415675 intron variant G/A;T snv 3
rs73720034 1.000 0.040 7 125794995 intergenic variant T/C snv 7.2E-02 3
rs74860738 0.925 0.040 11 80671683 intergenic variant G/A snv 7.2E-02 3
rs75995702 0.925 0.040 11 42785177 intergenic variant C/G;T snv 3
rs7613360 1.000 0.040 3 49879277 upstream gene variant C/T snv 0.32 3
rs78087832 0.925 0.040 2 224600060 intergenic variant C/T snv 2.4E-03 3
rs7939345 1.000 0.040 11 47959016 intergenic variant T/A;G snv 3
rs8100891 1.000 0.040 19 32338607 intergenic variant C/A;G snv 3
rs143405544
ADAMTS6
0.925 0.040 5 65459777 intron variant A/G snv 4.8E-03 3
rs1789891
ADH1B
1.000 0.080 4 99329262 intron variant C/A snv 0.13 3
rs35825582
ARHGAP15
1.000 0.040 2 143491193 intron variant G/A snv 0.45 3
rs188843168
ATP5MD
0.925 0.040 10 103390184 intron variant T/A;C snv 4.3E-04 3
rs77945277
BAZ1A
0.925 0.040 14 34840969 intron variant A/G snv 4.9E-03 3
rs138472420
BICRA
1.000 0.040 19 47657765 intron variant G/A snv 3.3E-03 3
rs6063349
CSE1L
0.925 0.040 20 49065345 intron variant G/A;C;T snv 3
rs142641502
CSTF3
0.925 0.040 11 33109861 intron variant T/C snv 8.0E-03 3
rs4839421
CYMP
0.925 0.040 1 110479338 intron variant C/A snv 0.40 3