rs11042950
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs11042950(A;A) |
Make rs11042950(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 2168488 |
Gene | TH |
is a | snp |
is | mentioned by |
dbSNP | rs11042950 |
dbSNP (classic) | rs11042950 |
ClinGen | rs11042950 |
ebi | rs11042950 |
HLI | rs11042950 |
Exac | rs11042950 |
Gnomad | rs11042950 |
Varsome | rs11042950 |
LitVar | rs11042950 |
Map | rs11042950 |
PheGenI | rs11042950 |
Biobank | rs11042950 |
1000 genomes | rs11042950 |
hgdp | rs11042950 |
ensembl | rs11042950 |
geneview | rs11042950 |
scholar | rs11042950 |
rs11042950 | |
pharmgkb | rs11042950 |
gwascentral | rs11042950 |
openSNP | rs11042950 |
23andMe | rs11042950 |
SNPshot | rs11042950 |
SNPdbe | rs11042950 |
MSV3d | rs11042950 |
GWAS Ctlg | rs11042950 |
GMAF | 0.002755 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 24275212] The role of tyrosine hydroxylase gene variants in suicide attempt in schizophrenia
ClinVar | |
---|---|
Risk | rs11042950(A;A) |
Alt | rs11042950(A;A) |
Reference | Rs11042950(G;G) |
Significance | Non-pathogenic |
Disease | Dystonia |
Variation | info |
Gene | TH |
CLNDBN | Dystonia |
Reversed | 1 |
HGVS | NC_000011.9:g.2189718C>T |
CLNSRC | |
CLNACC | RCV000229985.1, |