Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 10
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 5
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 5
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 5
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 5
rs11585926
TRIM33
1.000 0.040 1 114431068 intron variant T/C snv 0.22 3
rs11102800
TRIM33
1.000 0.040 1 114498310 intron variant C/T snv 0.58 2
rs4307059 0.882 0.080 5 25967594 intron variant T/A;C snv 2
rs4773054 1.000 0.040 13 109501681 intron variant T/C snv 0.89 2
rs10489525
CSDE1
1.000 0.040 1 114721064 intron variant G/A snv 0.32 1
rs10513025 1.000 0.040 5 9623510 non coding transcript exon variant T/C snv 5.4E-02 1
rs10858047 1.000 0.040 1 114531255 upstream gene variant T/C snv 0.13 1
rs11102807 1.000 0.040 1 114518963 intergenic variant A/G snv 0.44 1
rs11582563
TRIM33
1.000 0.040 1 114416918 intron variant G/A snv 0.14 1
rs11587400
PKMP1
1.000 0.040 1 114537037 non coding transcript exon variant C/G;T snv 1
rs11589568
TRIM33
1.000 0.040 1 114453702 intron variant T/C snv 0.14 1
rs12456492
RIT2
0.882 0.080 18 43093415 intron variant A/G snv 0.33 1
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 1
rs1409313
CUEDC2
1.000 0.040 10 102431844 intron variant T/C snv 0.85 1
rs16976358
LINC00907
0.827 0.080 18 42611606 intron variant T/C snv 1.0E-02 1
rs1858830
MET
0.925 0.040 7 116672385 5 prime UTR variant C/G snv 0.40 1
rs1877455 1.000 0.040 1 114556471 intergenic variant C/T snv 0.12 1
rs3827735
TRIM33
1.000 0.040 1 114510087 intron variant C/A;T snv 1
rs4141463
MACROD2
0.925 0.040 20 14766825 intron variant T/C snv 0.50 1
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 1