rs1364402
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1364402(C;C) |
Make rs1364402(C;T) |
Make rs1364402(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 136899616 |
Gene | CHRM2, LOC349160 |
is a | snp |
is | mentioned by |
dbSNP | rs1364402 |
dbSNP (classic) | rs1364402 |
ClinGen | rs1364402 |
ebi | rs1364402 |
HLI | rs1364402 |
Exac | rs1364402 |
Gnomad | rs1364402 |
Varsome | rs1364402 |
LitVar | rs1364402 |
Map | rs1364402 |
PheGenI | rs1364402 |
Biobank | rs1364402 |
1000 genomes | rs1364402 |
hgdp | rs1364402 |
ensembl | rs1364402 |
geneview | rs1364402 |
scholar | rs1364402 |
rs1364402 | |
pharmgkb | rs1364402 |
gwascentral | rs1364402 |
openSNP | rs1364402 |
23andMe | rs1364402 |
SNPshot | rs1364402 |
SNPdbe | rs1364402 |
MSV3d | rs1364402 |
GWAS Ctlg | rs1364402 |
GMAF | 0.1056 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23793025] |
Trait | Migraine with aura |
Title | Genome-wide meta-analysis identifies new susceptibility loci for migraine. |
Risk Allele | |
P-val | 4E-6 |
Odds Ratio | 1.19 [1.11-1.28] |
[PMID 17996044] Exploring the functional role of the CHRM2 gene in human cognition: results from a dense genotyping and brain expression study.