rs11974297
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 1 | Migraine |
Make rs11974297(A;A) |
Make rs11974297(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 50550562 |
Gene | DDC |
is a | snp |
is | mentioned by |
dbSNP | rs11974297 |
dbSNP (classic) | rs11974297 |
ClinGen | rs11974297 |
ebi | rs11974297 |
HLI | rs11974297 |
Exac | rs11974297 |
Gnomad | rs11974297 |
Varsome | rs11974297 |
LitVar | rs11974297 |
Map | rs11974297 |
PheGenI | rs11974297 |
Biobank | rs11974297 |
1000 genomes | rs11974297 |
hgdp | rs11974297 |
ensembl | rs11974297 |
geneview | rs11974297 |
scholar | rs11974297 |
rs11974297 | |
pharmgkb | rs11974297 |
gwascentral | rs11974297 |
openSNP | rs11974297 |
23andMe | rs11974297 |
SNPshot | rs11974297 |
SNPdbe | rs11974297 |
MSV3d | rs11974297 |
GWAS Ctlg | rs11974297 |
GMAF | 0.4784 |
Max Magnitude | 1 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19455600] a haplotype consisting of rs2329340(A), rs11974297(C), rs2044859(T) and rs11761683(G) associated with increased incidence of migraine with aura among a sample of 528 migraine patients (308 without aura, 220 with aura) and 528 sex-matched migraine-free controls