rs746164064
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs746164064(C;T) |
| Make rs746164064(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 19 |
| Position | 44705631 |
| Gene | CEACAM16, LOC107985305 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs746164064 |
| dbSNP (classic) | rs746164064 |
| ClinGen | rs746164064 |
| ebi | rs746164064 |
| HLI | rs746164064 |
| Exac | rs746164064 |
| Gnomad | rs746164064 |
| Varsome | rs746164064 |
| LitVar | rs746164064 |
| Map | rs746164064 |
| PheGenI | rs746164064 |
| Biobank | rs746164064 |
| 1000 genomes | rs746164064 |
| hgdp | rs746164064 |
| ensembl | rs746164064 |
| geneview | rs746164064 |
| scholar | rs746164064 |
| rs746164064 | |
| pharmgkb | rs746164064 |
| gwascentral | rs746164064 |
| openSNP | rs746164064 |
| 23andMe | rs746164064 |
| SNPshot | rs746164064 |
| SNPdbe | rs746164064 |
| MSV3d | rs746164064 |
| GWAS Ctlg | rs746164064 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs746164064(T;T) |
| Alt | rs746164064(T;T) |
| Reference | Rs746164064(C;C) |
| Significance | Pathogenic |
| Disease | Nonsyndromic hearing loss and deafness |
| Variation | info |
| Gene | CEACAM16 |
| CLNDBN | Nonsyndromic hearing loss and deafness |
| Reversed | 0 |
| HGVS | NC_000019.9:g.45208901C>T |
| CLNSRC | |
| CLNACC | RCV000225009.1, |
