rs35219372
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs35219372(A;A) |
| Make rs35219372(A;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 22 |
| Position | 19971288 |
| Gene | ARVCF |
| is a | snp |
| is | mentioned by |
| dbSNP | rs35219372 |
| dbSNP (classic) | rs35219372 |
| ClinGen | rs35219372 |
| ebi | rs35219372 |
| HLI | rs35219372 |
| Exac | rs35219372 |
| Gnomad | rs35219372 |
| Varsome | rs35219372 |
| LitVar | rs35219372 |
| Map | rs35219372 |
| PheGenI | rs35219372 |
| Biobank | rs35219372 |
| 1000 genomes | rs35219372 |
| hgdp | rs35219372 |
| ensembl | rs35219372 |
| geneview | rs35219372 |
| scholar | rs35219372 |
| rs35219372 | |
| pharmgkb | rs35219372 |
| gwascentral | rs35219372 |
| openSNP | rs35219372 |
| 23andMe | rs35219372 |
| SNPshot | rs35219372 |
| SNPdbe | rs35219372 |
| MSV3d | rs35219372 |
| GWAS Ctlg | rs35219372 |
| GMAF | 0.009183 |
| Max Magnitude | 0 |
[PMID 20333729
] A functional variant provided further evidence for the association of ARVCF with schizophrenia
