rs11178998
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs11178998(A;G) |
Make rs11178998(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 71938935 |
Gene | TPH2 |
is a | snp |
is | mentioned by |
dbSNP | rs11178998 |
dbSNP (classic) | rs11178998 |
ClinGen | rs11178998 |
ebi | rs11178998 |
HLI | rs11178998 |
Exac | rs11178998 |
Gnomad | rs11178998 |
Varsome | rs11178998 |
LitVar | rs11178998 |
Map | rs11178998 |
PheGenI | rs11178998 |
Biobank | rs11178998 |
1000 genomes | rs11178998 |
hgdp | rs11178998 |
ensembl | rs11178998 |
geneview | rs11178998 |
scholar | rs11178998 |
rs11178998 | |
pharmgkb | rs11178998 |
gwascentral | rs11178998 |
openSNP | rs11178998 |
23andMe | rs11178998 |
SNPshot | rs11178998 |
SNPdbe | rs11178998 |
MSV3d | rs11178998 |
GWAS Ctlg | rs11178998 |
GMAF | 0.08724 |
Max Magnitude | 0 |
[PMID 18797398] Investigation of the tryptophan hydroxylase 2 gene in bipolar I disorder in the Romanian population. [PMID 22655589] Investigation of tryptophan hydroxylase 2 (TPH2) in schizophrenia and in the response to antipsychotics.
ClinVar | |
---|---|
Risk | rs11178998(G;G) |
Alt | rs11178998(G;G) |
Reference | Rs11178998(A;A) |
Significance | Probable-non-pathogenic |
Disease | Tryptophan 5-monooxygenase deficiency |
Variation | info |
Gene | TPH2 |
CLNDBN | Tryptophan 5-monooxygenase deficiency |
Reversed | 0 |
HGVS | NC_000012.11:g.72332715A>G |
CLNSRC | |
CLNACC | RCV000387456.1, |