rs189754995
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs189754995(G;T) |
| Make rs189754995(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 6 |
| Position | 70255375 |
| Gene | COL9A1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs189754995 |
| dbSNP (classic) | rs189754995 |
| ClinGen | rs189754995 |
| ebi | rs189754995 |
| HLI | rs189754995 |
| Exac | rs189754995 |
| Gnomad | rs189754995 |
| Varsome | rs189754995 |
| LitVar | rs189754995 |
| Map | rs189754995 |
| PheGenI | rs189754995 |
| Biobank | rs189754995 |
| 1000 genomes | rs189754995 |
| hgdp | rs189754995 |
| ensembl | rs189754995 |
| geneview | rs189754995 |
| scholar | rs189754995 |
| rs189754995 | |
| pharmgkb | rs189754995 |
| gwascentral | rs189754995 |
| openSNP | rs189754995 |
| 23andMe | rs189754995 |
| SNPshot | rs189754995 |
| SNPdbe | rs189754995 |
| MSV3d | rs189754995 |
| GWAS Ctlg | rs189754995 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs189754995(A;A) rs189754995(T;T) |
| Alt | rs189754995(A;A) rs189754995(T;T) |
| Reference | Rs189754995(G;G) |
| Significance | Pathogenic |
| Disease | Stickler syndrome |
| Variation | info |
| Gene | COL9A1 |
| CLNDBN | Stickler syndrome, type 4 |
| Reversed | 0 |
| HGVS | NC_000006.11:g.70965078G>A |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000148951.2, |
