rs4446909
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4446909(A;A) |
| Make rs4446909(A;G) |
| Make rs4446909(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | X |
| Position | 1614890 |
| Gene | ASMT |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4446909 |
| dbSNP (classic) | rs4446909 |
| ClinGen | rs4446909 |
| ebi | rs4446909 |
| HLI | rs4446909 |
| Exac | rs4446909 |
| Gnomad | rs4446909 |
| Varsome | rs4446909 |
| LitVar | rs4446909 |
| Map | rs4446909 |
| PheGenI | rs4446909 |
| Biobank | rs4446909 |
| 1000 genomes | rs4446909 |
| hgdp | rs4446909 |
| ensembl | rs4446909 |
| geneview | rs4446909 |
| scholar | rs4446909 |
| rs4446909 | |
| pharmgkb | rs4446909 |
| gwascentral | rs4446909 |
| openSNP | rs4446909 |
| 23andMe | rs4446909 |
| SNPshot | rs4446909 |
| SNPdbe | rs4446909 |
| MSV3d | rs4446909 |
| GWAS Ctlg | rs4446909 |
| GMAF | 0.1979 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 21827647
] Polymorphisms in melatonin synthesis pathways: possible influences on depression
[PMID 17505466] Abnormal melatonin synthesis in autism spectrum disorders.
[PMID 20433639] Single-nucleotide polymorphisms and mRNA expression for melatonin synthesis rate-limiting enzyme in recurrent depressive disorder.
