rs165849
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs165849(A;A) |
| Make rs165849(A;G) |
| Make rs165849(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 19971146 |
| Gene | ARVCF |
| is a | snp |
| is | mentioned by |
| dbSNP | rs165849 |
| dbSNP (classic) | rs165849 |
| ClinGen | rs165849 |
| ebi | rs165849 |
| HLI | rs165849 |
| Exac | rs165849 |
| Gnomad | rs165849 |
| Varsome | rs165849 |
| LitVar | rs165849 |
| Map | rs165849 |
| PheGenI | rs165849 |
| Biobank | rs165849 |
| 1000 genomes | rs165849 |
| hgdp | rs165849 |
| ensembl | rs165849 |
| geneview | rs165849 |
| scholar | rs165849 |
| rs165849 | |
| pharmgkb | rs165849 |
| gwascentral | rs165849 |
| openSNP | rs165849 |
| 23andMe | rs165849 |
| SNPshot | rs165849 |
| SNPdbe | rs165849 |
| MSV3d | rs165849 |
| GWAS Ctlg | rs165849 |
| GMAF | 0.4803 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20333729
] A functional variant provided further evidence for the association of ARVCF with schizophrenia
[PMID 19508883] ARVCF single marker and haplotypic association with schizophrenia
[PMID 15340358] Haplotypic association spanning the 22q11.21 genes COMT and ARVCF with schizophrenia.
[PMID 16232322] COMT genetic variation confers risk for psychotic and affective disorders: a case control study.
[PMID 19015200] Polymorphisms in estrogen- and androgen-metabolizing genes and the risk of gastric cancer.
[PMID 19329282] Meta-analysis of association between genetic variants in COMT and schizophrenia: an update.
