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
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 11
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9
rs740746 10 114033028 intergenic variant G/A snv 0.70 8
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
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
rs10409243
S1PR2 ; DNMT1
19 10222312 3 prime UTR variant C/A;G;T snv 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
rs55872725
FTO
16 53775211 intron variant C/T snv 0.31 6
rs62434129
PLEKHG1
6 150687701 intron variant A/G;T snv 8.8E-02 6
rs72681869
SOS2
14 50188639 missense variant G/A;C snv 4.0E-06; 4.1E-03 6
rs10184428 2 164155317 intron variant C/A;G snv 5
rs1126930
PRKAG1 ; DDN-AS1
12 49005349 missense variant G/C snv 2.1E-02 2.1E-02 5
rs11636952
LMAN1L
15 74821981 intron variant T/C snv 0.48 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