rs2078371
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2078371(C;C) |
Make rs2078371(C;T) |
Make rs2078371(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 115134562 |
is a | snp |
is | mentioned by |
dbSNP | rs2078371 |
dbSNP (classic) | rs2078371 |
ClinGen | rs2078371 |
ebi | rs2078371 |
HLI | rs2078371 |
Exac | rs2078371 |
Gnomad | rs2078371 |
Varsome | rs2078371 |
LitVar | rs2078371 |
Map | rs2078371 |
PheGenI | rs2078371 |
Biobank | rs2078371 |
1000 genomes | rs2078371 |
hgdp | rs2078371 |
ensembl | rs2078371 |
geneview | rs2078371 |
scholar | rs2078371 |
rs2078371 | |
pharmgkb | rs2078371 |
gwascentral | rs2078371 |
openSNP | rs2078371 |
23andMe | rs2078371 |
SNPshot | rs2078371 |
SNPdbe | rs2078371 |
MSV3d | rs2078371 |
GWAS Ctlg | rs2078371 |
GMAF | 0.1267 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 23294458] Replication and meta-analysis of common variants identifies a genome-wide significant locus in migraine
[PMID 30256423] Using a Genetic Risk Score Approach to Predict Headache Response to Triptans in Migraine Without Aura.