rs887199
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs887199(A;A) |
| Make rs887199(A;G) |
| Make rs887199(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 19974432 |
| Gene | ARVCF |
| is a | snp |
| is | mentioned by |
| dbSNP | rs887199 |
| dbSNP (classic) | rs887199 |
| ClinGen | rs887199 |
| ebi | rs887199 |
| HLI | rs887199 |
| Exac | rs887199 |
| Gnomad | rs887199 |
| Varsome | rs887199 |
| LitVar | rs887199 |
| Map | rs887199 |
| PheGenI | rs887199 |
| Biobank | rs887199 |
| 1000 genomes | rs887199 |
| hgdp | rs887199 |
| ensembl | rs887199 |
| geneview | rs887199 |
| scholar | rs887199 |
| rs887199 | |
| pharmgkb | rs887199 |
| gwascentral | rs887199 |
| openSNP | rs887199 |
| 23andMe | rs887199 |
| SNPshot | rs887199 |
| SNPdbe | rs887199 |
| MSV3d | rs887199 |
| GWAS Ctlg | rs887199 |
| GMAF | 0.3416 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19508883] ARVCF single marker and haplotypic association with schizophrenia
[PMID 18574484
] The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase.
