rs17551608
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17551608(C;C) |
| Make rs17551608(C;T) |
| Make rs17551608(T;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 5 |
| Position | 168408534 |
| Gene | WWC1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17551608 |
| dbSNP (classic) | rs17551608 |
| ClinGen | rs17551608 |
| ebi | rs17551608 |
| HLI | rs17551608 |
| Exac | rs17551608 |
| Gnomad | rs17551608 |
| Varsome | rs17551608 |
| LitVar | rs17551608 |
| Map | rs17551608 |
| PheGenI | rs17551608 |
| Biobank | rs17551608 |
| 1000 genomes | rs17551608 |
| hgdp | rs17551608 |
| ensembl | rs17551608 |
| geneview | rs17551608 |
| scholar | rs17551608 |
| rs17551608 | |
| pharmgkb | rs17551608 |
| gwascentral | rs17551608 |
| openSNP | rs17551608 |
| 23andMe | rs17551608 |
| SNPshot | rs17551608 |
| SNPdbe | rs17551608 |
| MSV3d | rs17551608 |
| GWAS Ctlg | rs17551608 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 26405221
] Exome Sequence Data From Multigenerational Families Implicate AMPA Receptor Trafficking in Neurocognitive Impairment and Schizophrenia Risk
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 5
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
