rs8766
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs8766(A;G) |
| Make rs8766(G;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 18 |
| Position | 55228300 |
| Gene | TCF4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs8766 |
| dbSNP (classic) | rs8766 |
| ClinGen | rs8766 |
| ebi | rs8766 |
| HLI | rs8766 |
| Exac | rs8766 |
| Gnomad | rs8766 |
| Varsome | rs8766 |
| LitVar | rs8766 |
| Map | rs8766 |
| PheGenI | rs8766 |
| Biobank | rs8766 |
| 1000 genomes | rs8766 |
| hgdp | rs8766 |
| ensembl | rs8766 |
| geneview | rs8766 |
| scholar | rs8766 |
| rs8766 | |
| pharmgkb | rs8766 |
| gwascentral | rs8766 |
| openSNP | rs8766 |
| 23andMe | rs8766 |
| SNPshot | rs8766 |
| SNPdbe | rs8766 |
| MSV3d | rs8766 |
| GWAS Ctlg | rs8766 |
| Max Magnitude | 0 |
[PMID 27305091] Genetic Association of TCF4 and AKT1 Gene Variants with the Age at Onset of Schizophrenia.
| ClinVar | |
|---|---|
| Risk | rs8766(G;G) |
| Alt | rs8766(G;G) |
| Reference | Rs8766(A;A) |
| Significance | Non-pathogenic |
| Disease | not specified Pitt-Hopkins syndrome |
| Variation | info |
| Gene | TCF4 |
| CLNDBN | not specified Pitt-Hopkins syndrome |
| Reversed | 1 |
| HGVS | NC_000018.9:g.52895531T>C |
| CLNSRC | |
| CLNACC | RCV000079460.8, RCV000405030.1, |
[PMID 30288643] TCF4 and GRM8 gene polymorphisms and risk of schizophrenia in an Iranian population: a case-control study.
