Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 10
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 5
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 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
rs11585926
TRIM33
1.000 0.040 1 114431068 intron variant T/C snv 0.22 3
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
rs11102800
TRIM33
1.000 0.040 1 114498310 intron variant C/T snv 0.58 2
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
rs1877455 1.000 0.040 1 114556471 intergenic variant C/T snv 0.12 1
rs4327572 0.882 0.120 5 25972712 intron variant C/T snv 0.28 1
rs6894838 0.925 0.080 5 25944837 intergenic variant T/C snv 0.63 1
rs7834018 1.000 0.040 8 71649507 intergenic variant C/T snv 0.83 1
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 1
rs926938
AMPD1
1.000 0.040 1 114697195 upstream gene variant A/G;T snv 1
rs4765905
CACNA1C
0.827 0.040 12 2240418 intron variant G/A;C snv 1
rs10489525
CSDE1
1.000 0.040 1 114721064 intron variant G/A snv 0.32 1
rs8453
CSDE1 ; NRAS
1.000 0.040 1 114716978 3 prime UTR variant G/T snv 0.11 1
rs1409313
CUEDC2
1.000 0.040 10 102431844 intron variant T/C snv 0.85 1