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
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 11
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs740746 10 114033028 intergenic variant G/A snv 0.70 8
rs2306363
SIPA1
11 65638129 5 prime UTR variant G/T snv 0.15 7
rs10255839
EVX1
7 27249498 intron variant G/A snv 0.87 6
rs11099097 4 80246155 intergenic variant C/T snv 0.30 6
rs1290784
MECOM
3 169379112 intron variant C/A;T snv 6
rs13125101 4 80253438 TF binding site variant G/A snv 0.24 6
rs17030613
CAPZA1
1 112648185 intron variant A/C snv 0.19 6
rs17035646
CASZ1
1 10736490 intron variant G/A;T snv 6
rs1887320 20 10985350 intron variant G/A snv 0.46 6
rs2643826 3 27521497 upstream gene variant C/T snv 0.56 6
rs62434129
PLEKHG1
6 150687701 intron variant A/G;T snv 8.8E-02 6
rs10059884 5 32832368 regulatory region variant C/A;T snv 5
rs10184428 2 164155317 intron variant C/A;G snv 5
rs11725969
GUCY1A1
4 155705436 intron variant C/T snv 0.24 5
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 5
rs12978472
INSR
19 7257979 intron variant C/G;T snv 5
rs13149993 4 80237391 regulatory region variant G/A;C snv 5
rs1573643
FURIN
15 90877743 intron variant T/C snv 0.33 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