rs35441529
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (-;-) | 0 | common in clinvar |
| Make rs35441529(-;C) |
| Make rs35441529(C;C) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 6 |
| Position | 157206688 |
| Gene | ARID1B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs35441529 |
| dbSNP (classic) | rs35441529 |
| ClinGen | rs35441529 |
| ebi | rs35441529 |
| HLI | rs35441529 |
| Exac | rs35441529 |
| Gnomad | rs35441529 |
| Varsome | rs35441529 |
| LitVar | rs35441529 |
| Map | rs35441529 |
| PheGenI | rs35441529 |
| Biobank | rs35441529 |
| 1000 genomes | rs35441529 |
| hgdp | rs35441529 |
| ensembl | rs35441529 |
| geneview | rs35441529 |
| scholar | rs35441529 |
| rs35441529 | |
| pharmgkb | rs35441529 |
| gwascentral | rs35441529 |
| openSNP | rs35441529 |
| 23andMe | rs35441529 |
| SNPshot | rs35441529 |
| SNPdbe | rs35441529 |
| MSV3d | rs35441529 |
| GWAS Ctlg | rs35441529 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs35441529(C;C) |
| Alt | rs35441529(C;C) |
| Reference | Rs35441529(-;-) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | ARID1B |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000006.11:g.157527822dupC |
| CLNSRC | |
| CLNACC | RCV000359978.1, |
