rs4363087
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4363087(C;C) |
Make rs4363087(C;T) |
Make rs4363087(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 73703866 |
Gene | LOC105375350, STX1A |
is a | snp |
is | mentioned by |
dbSNP | rs4363087 |
dbSNP (classic) | rs4363087 |
ClinGen | rs4363087 |
ebi | rs4363087 |
HLI | rs4363087 |
Exac | rs4363087 |
Gnomad | rs4363087 |
Varsome | rs4363087 |
LitVar | rs4363087 |
Map | rs4363087 |
PheGenI | rs4363087 |
Biobank | rs4363087 |
1000 genomes | rs4363087 |
hgdp | rs4363087 |
ensembl | rs4363087 |
geneview | rs4363087 |
scholar | rs4363087 |
rs4363087 | |
pharmgkb | rs4363087 |
gwascentral | rs4363087 |
openSNP | rs4363087 |
23andMe | rs4363087 |
SNPshot | rs4363087 |
SNPdbe | rs4363087 |
MSV3d | rs4363087 |
GWAS Ctlg | rs4363087 |
GMAF | 0.3884 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 19368856] Contribution of syntaxin 1A to the genetic susceptibility to migraine: A case -- control association study in the Spanish population
[PMID 22250207] Association analysis of STX1A gene variants in common forms of migraine.
[PMID 23572023] Clinical and molecular characterization of the potential CF disease modifier syntaxin 1A