rs12249377
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12249377(A;A) |
Make rs12249377(A;C) |
Make rs12249377(C;C) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 90833199 |
Gene | HTR7 |
is a | snp |
is | mentioned by |
dbSNP | rs12249377 |
dbSNP (classic) | rs12249377 |
ClinGen | rs12249377 |
ebi | rs12249377 |
HLI | rs12249377 |
Exac | rs12249377 |
Gnomad | rs12249377 |
Varsome | rs12249377 |
LitVar | rs12249377 |
Map | rs12249377 |
PheGenI | rs12249377 |
Biobank | rs12249377 |
1000 genomes | rs12249377 |
hgdp | rs12249377 |
ensembl | rs12249377 |
geneview | rs12249377 |
scholar | rs12249377 |
rs12249377 | |
pharmgkb | rs12249377 |
gwascentral | rs12249377 |
openSNP | rs12249377 |
23andMe | rs12249377 |
SNPshot | rs12249377 |
SNPdbe | rs12249377 |
MSV3d | rs12249377 |
GWAS Ctlg | rs12249377 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24736177![]() |
Trait | White matter microstructure (global fractional anisotropy) |
Title | Common genetic variants and gene expression associated with white matter microstructure in the human brain. |
Risk Allele | |
P-val | 3E-10 |
Odds Ratio | NR NR |