rs10840491
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10840491(A;A) |
Make rs10840491(A;G) |
Make rs10840491(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 2173160 |
Gene | MIR4686, TH |
is a | snp |
is | mentioned by |
dbSNP | rs10840491 |
dbSNP (classic) | rs10840491 |
ClinGen | rs10840491 |
ebi | rs10840491 |
HLI | rs10840491 |
Exac | rs10840491 |
Gnomad | rs10840491 |
Varsome | rs10840491 |
LitVar | rs10840491 |
Map | rs10840491 |
PheGenI | rs10840491 |
Biobank | rs10840491 |
1000 genomes | rs10840491 |
hgdp | rs10840491 |
ensembl | rs10840491 |
geneview | rs10840491 |
scholar | rs10840491 |
rs10840491 | |
pharmgkb | rs10840491 |
gwascentral | rs10840491 |
openSNP | rs10840491 |
23andMe | rs10840491 |
SNPshot | rs10840491 |
SNPdbe | rs10840491 |
MSV3d | rs10840491 |
GWAS Ctlg | rs10840491 |
GMAF | 0.1451 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
Tyrosine hydroxylase Val81Met polymorphism: lack of association with schizophrenia. [PMID 19491717]
[PMID 19956101] Overview of the Rapid Response data.