Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10405744
ZNF93
0.851 0.040 19 19948684 intron variant G/A snv 9.0E-02 4
rs10968749
LINGO2
0.851 0.040 9 28752486 intergenic variant A/G snv 5.5E-02 4
rs11829119
LOC107984527
0.851 0.040 12 19040597 intergenic variant T/A;C snv 4
rs16875288
ADAMTS16 ; LOC101929200
0.851 0.040 5 5297087 intron variant A/T snv 0.22 4
rs16935279
LINC01592
0.851 0.040 8 68961217 intron variant T/C snv 1.9E-02 4
rs17066873 0.851 0.040 13 76889874 non coding transcript exon variant T/C snv 5.4E-02 4
rs17154917 0.851 0.040 7 81207393 intergenic variant G/A;T snv 4
rs17158930
DOCK4
0.851 0.040 7 111871082 intron variant A/G snv 0.25 4
rs17211233
RASGRF2
0.882 0.040 5 81072944 intron variant T/A;C snv 4
rs17673138
NRG1
0.851 0.040 8 32840440 intron variant A/C snv 8.6E-02 4
rs17790731
RFESD
0.851 0.040 5 95647825 5 prime UTR variant C/T snv 4.9E-02 4
rs2302045
MTERF4 ; SNED1
0.851 0.040 2 241081801 splice region variant G/A snv 7.6E-02 1.0E-01 4
rs55945116
SEC11A
0.882 0.040 15 84676882 intron variant G/C snv 0.26 4
rs6586354 0.851 0.040 1 234897489 intron variant G/A snv 0.25 4
rs9862857
LOC101927995 ; LOC105377013
0.851 0.040 3 30453840 regulatory region variant A/G;T snv 4
rs11082011
CELF4
0.925 0.040 18 37565159 intron variant C/T snv 0.53 3
rs111365677 0.925 0.040 1 99463578 upstream gene variant T/C snv 2.3E-03 3
rs11155372
UTRN
0.925 0.040 6 144698602 intron variant G/C;T snv 3
rs112106319
TNC ; DELEC1
0.925 0.040 9 115094539 intron variant A/T snv 2.8E-03 3
rs112538845 0.925 0.040 4 184084475 downstream gene variant C/T snv 1.7E-02 3
rs11591827 0.925 0.040 10 81128126 intergenic variant G/A snv 8.4E-02 3
rs11728985
C4orf33
0.925 0.040 4 129115280 3 prime UTR variant C/T snv 0.12 3
rs11924809
DGKG
0.925 0.040 3 186353656 intron variant G/A snv 5.3E-02 3
rs11990063
MSRA
0.925 0.040 8 10307685 intron variant C/A;T snv 3
rs12555870 0.925 0.040 9 23347726 intron variant A/G snv 0.36 3