rs11594111
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11594111(A;A) |
Make rs11594111(A;G) |
Make rs11594111(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 14903407 |
Gene | DCLRE1C, SUV39H2 |
is a | snp |
is | mentioned by |
dbSNP | rs11594111 |
dbSNP (classic) | rs11594111 |
ClinGen | rs11594111 |
ebi | rs11594111 |
HLI | rs11594111 |
Exac | rs11594111 |
Gnomad | rs11594111 |
Varsome | rs11594111 |
LitVar | rs11594111 |
Map | rs11594111 |
PheGenI | rs11594111 |
Biobank | rs11594111 |
1000 genomes | rs11594111 |
hgdp | rs11594111 |
ensembl | rs11594111 |
geneview | rs11594111 |
scholar | rs11594111 |
rs11594111 | |
pharmgkb | rs11594111 |
gwascentral | rs11594111 |
openSNP | rs11594111 |
23andMe | rs11594111 |
SNPshot | rs11594111 |
SNPdbe | rs11594111 |
MSV3d | rs11594111 |
GWAS Ctlg | rs11594111 |
GMAF | 0.06566 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23793025] |
Trait | Migraine |
Title | Genome-wide meta-analysis identifies new susceptibility loci for migraine. |
Risk Allele | G |
P-val | 1E-7 |
Odds Ratio | 1.09 [1.06-1.12] |