Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 23
rs17030613
CAPZA1
1 112648185 intron variant A/C snv 0.19 6
rs1887320 20 10985350 intron variant G/A snv 0.46 6
rs2643826 3 27521497 upstream gene variant C/T snv 0.56 6
rs10184428 2 164155317 intron variant C/A;G snv 5
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 5
rs13149993 4 80237391 regulatory region variant G/A;C snv 5
rs167479
RGL3
19 11416089 missense variant T/A;C;G snv 5
rs16896398
SLC22A7
6 43294966 upstream gene variant A/T snv 0.42 5
rs1731249
KCNK3
2 26697157 intron variant T/A snv 0.48 5
rs35443 12 115115073 intergenic variant G/C snv 0.40 5
rs35444 12 115114632 intergenic variant A/G snv 0.38 5
rs3790604
WNT2B
1 112504257 intron variant C/A snv 7.8E-02 5
rs4980389
LSP1
11 1871355 5 prime UTR variant G/A snv 0.35 5
rs8068318
TBX2
17 61406405 non coding transcript exon variant C/T snv 0.56 5
rs10776752
WNT2B
1 112501706 intron variant G/T snv 8.8E-02 4
rs10948071
ZNF318
6 43312975 intron variant C/T snv 0.46 4
rs11105364
ATP2B1
12 89675499 intron variant T/G snv 0.15 4
rs12129649
MOV10
1 112688881 5 prime UTR variant G/T snv 6.6E-02 4
rs12630213
FGD5
3 14912904 intron variant C/T snv 0.68 4
rs1401982
ATP2B1
12 89595822 intron variant G/A snv 0.60 4
rs1563788
ZNF318
6 43340625 intron variant C/T snv 0.42 4
rs16849225 2 164050310 intron variant C/T snv 0.19 4
rs17004869
FGF5
4 80283879 intron variant A/T snv 4.6E-02 4
rs1731243
KCNK3
2 26707543 intron variant C/T snv 0.48 4