Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11124945
PLEKHH2
1.000 0.040 2 43650017 intron variant A/G snv 0.21 3
rs11191514
CNNM2
10 103013607 intron variant C/G;T snv 1
rs11191548
CNNM2
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02 4
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 10
rs11191593
NT5C2
10 103179458 intron variant T/C snv 9.0E-02 3
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 4
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 3
rs11229457
OR5B12
11 58439730 missense variant C/G;T snv 0.21 0.22 3
rs11230728
LRRC10B
11 61510226 3 prime UTR variant A/G snv 0.13 1
rs1126464
DPEP1
1.000 0.040 16 89637957 missense variant G/A;C snv 1.3E-05; 0.26 4
rs1126478
LTF
0.763 0.240 3 46459723 missense variant T/C snv 0.41 0.51 1
rs112913898 10 103199143 intergenic variant G/A snv 9.1E-02 3
rs113296370
PLEKHH2
1.000 0.040 2 43636315 upstream gene variant A/C snv 0.17 3
rs115236533
CDH18
5 19745606 intron variant G/C snv 3.9E-03 3
rs11537751
NDUFS3 ; PTPMT1 ; CELF1
11 47565900 missense variant C/T snv 3.7E-02 3.6E-02 1
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 13
rs11563582 7 27312031 intergenic variant G/A snv 9.8E-02 3
rs11568818
MMP7
0.763 0.280 11 102530930 upstream gene variant T/A;C snv 1
rs115706913
SGCZ
8 14224308 intron variant T/C snv 2.7E-02 1
rs115795127
FRMD3
9 83378986 intron variant T/C snv 3.4E-02 3
rs11613352
R3HDM2
0.827 0.160 12 57398797 intron variant C/T snv 0.19 3
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 1
rs117353193
TCN2
0.925 0.080 22 30614430 missense variant G/A snv 7.1E-04 3.1E-04 2
rs1173766 5 32804422 intergenic variant T/C snv 0.57 3
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 5