Annotation Detail
Information
- Associated Genes
- OCA2
- Associated Variants
-
OCA2 c.1842+1G>T
(
ENST00000353809.9,
ENST00000354638.8 )
OCA2 c.1842+1G>T ( ENST00000353809.9, ENST00000354638.8 ) - Associated Disease
- oculocutaneous albinism
- Source Database
- ClinVar
- Description
- NM_000275.3(OCA2):c.1842+1G>T AND Oculocutaneous albinism
- ClinVar Allele ID
- 15992
- ClinVar RefSeq Alternation Syntax
- NM_001300984.2:c.1770+1G>T
- ClinVar RefSeq Alternation Syntax
- NM_000275.3:c.1842+1G>T
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2023-07-31
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003323345
- ClinVar Disease
- Oculocutaneous albinism
- Observed Origin Sample
- germline
Drugs