rs8192466
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common |
| (C;T) | 2.5 | uncertain, probably harmless |
| (T;T) | 4 | uncertain |
| Reference | GRCh38 38.1/142 |
| Chromosome | 11 |
| Position | 27658560 |
| Gene | BDNF, BDNF-AS |
| is a | snp |
| is | mentioned by |
| dbSNP | rs8192466 |
| dbSNP (classic) | rs8192466 |
| ClinGen | rs8192466 |
| ebi | rs8192466 |
| HLI | rs8192466 |
| Exac | rs8192466 |
| Gnomad | rs8192466 |
| Varsome | rs8192466 |
| LitVar | rs8192466 |
| Map | rs8192466 |
| PheGenI | rs8192466 |
| Biobank | rs8192466 |
| 1000 genomes | rs8192466 |
| hgdp | rs8192466 |
| ensembl | rs8192466 |
| geneview | rs8192466 |
| scholar | rs8192466 |
| rs8192466 | |
| pharmgkb | rs8192466 |
| gwascentral | rs8192466 |
| openSNP | rs8192466 |
| 23andMe | rs8192466 |
| SNPshot | rs8192466 |
| SNPdbe | rs8192466 |
| MSV3d | rs8192466 |
| GWAS Ctlg | rs8192466 |
| GMAF | 0.001377 |
| Max Magnitude | 4 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| ClinVar | |
|---|---|
| Risk | rs8192466(A;A) Rs8192466(T;T) |
| Alt | rs8192466(A;A) Rs8192466(T;T) |
| Reference | Rs8192466(C;C) |
| Significance | Pathogenic |
| Disease | Congenital central hypoventilation |
| Variation | info |
| Gene | BDNF-AS BDNF |
| CLNDBN | Congenital central hypoventilation |
| Reversed | 1 |
| HGVS | NC_000011.9:g.27680107G>A |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000019266.28, |
[PMID 17212826
] TAMGeS: a Three-array Method for Genotyping of SNPs by a dual-colour approach.
[PMID 17894414
] BDNF Val66Met variant and age of onset in schizophrenia.
