rs8150
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs8150(C;G) |
| Make rs8150(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 76470935 |
| Gene | AANAT, RHBDF2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs8150 |
| dbSNP (classic) | rs8150 |
| ClinGen | rs8150 |
| ebi | rs8150 |
| HLI | rs8150 |
| Exac | rs8150 |
| Gnomad | rs8150 |
| Varsome | rs8150 |
| LitVar | rs8150 |
| Map | rs8150 |
| PheGenI | rs8150 |
| Biobank | rs8150 |
| 1000 genomes | rs8150 |
| hgdp | rs8150 |
| ensembl | rs8150 |
| geneview | rs8150 |
| scholar | rs8150 |
| rs8150 | |
| pharmgkb | rs8150 |
| gwascentral | rs8150 |
| openSNP | rs8150 |
| 23andMe | rs8150 |
| SNPshot | rs8150 |
| SNPdbe | rs8150 |
| MSV3d | rs8150 |
| GWAS Ctlg | rs8150 |
| GMAF | 0.3898 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20459461] Resequencing and association analysis of arylalkylamine N-acetyltransferase (AANAT) gene and its contribution to major depression susceptibility
[PMID 19184136
] Examination of association of genes in the serotonin system to autism.
[PMID 25229211] Polymorphisms in circadian genes, night work and breast cancer: results from the GENICA study
| ClinVar | |
|---|---|
| Risk | rs8150(G;G) rs8150(T;T) |
| Alt | rs8150(G;G) rs8150(T;T) |
| Reference | Rs8150(C;C) |
| Significance | Non-pathogenic |
| Disease | Howel-Evans syndrome |
| Variation | info |
| Gene | RHBDF2 |
| CLNDBN | Howel-Evans syndrome |
| Reversed | 1 |
| HGVS | NC_000017.10:g.74467017G>C |
| CLNSRC | |
| CLNACC | RCV000284468.1, |
