Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs56388524 0.925 0.040 5 45757459 intergenic variant C/A;T snv 2.0E-02 3
rs6546604 0.925 0.040 2 70415675 intron variant G/A;T snv 3
rs74860738 0.925 0.040 11 80671683 intergenic variant G/A snv 7.2E-02 3
rs7555693 0.925 0.040 1 106295917 intergenic variant G/A snv 0.45 3
rs75995702 0.925 0.040 11 42785177 intergenic variant C/G;T snv 3
rs77826363 0.882 0.040 6 1128802 intergenic variant G/T snv 2.2E-02 3
rs78087832 0.925 0.040 2 224600060 intergenic variant C/T snv 2.4E-03 3
rs7828021 0.925 0.040 8 49727454 intergenic variant C/G;T snv 3
rs9364726 0.882 0.040 6 164236705 intergenic variant A/G snv 6.5E-02 3
rs143405544
ADAMTS6
0.925 0.040 5 65459777 intron variant A/G snv 4.8E-03 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
rs11728985
C4orf33
0.925 0.040 4 129115280 3 prime UTR variant C/T snv 0.12 3
rs11082011
CELF4
0.925 0.040 18 37565159 intron variant C/T snv 0.53 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
rs5743467
DEFB1
0.925 0.040 8 6874007 intron variant C/G snv 0.19 3
rs11924809
DGKG
0.925 0.040 3 186353656 intron variant G/A snv 5.3E-02 3
rs201203751
FYB1
0.925 0.040 5 39203496 intron variant TT/-;T;TTT delins 3
rs189864513
LINC01618
0.925 0.040 4 52767390 intron variant T/C snv 1.9E-03 3
rs55679149
LOC105378841
0.925 0.040 1 89068655 upstream gene variant C/T snv 0.34 3
rs34177316
LOC107986273 ; APBB2
0.925 0.040 4 40985283 intron variant A/-;AA;AAA delins 3
rs11990063
MSRA
0.925 0.040 8 10307685 intron variant C/A;T snv 3
rs73425402
NAV3
0.925 0.040 12 77503518 intron variant T/A snv 4.1E-02 3