NM_001110219.3(GJB6):c.594G>A (p.Ala198=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 26, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003095962.4
Allele description [Variation Report for NM_001110219.3(GJB6):c.594G>A (p.Ala198=)]
NM_001110219.3(GJB6):c.594G>A (p.Ala198=)
Condition(s)
- Name:
- Autosomal recessive nonsyndromic hearing loss 1A (DFNB1A)
- Synonyms:
- Deafness nonsyndromic, Connexin 26 linked; Deafness, autosomal recessive 1A; DFNB 1 Nonsyndromic Hearing Loss and Deafness; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0009076; MedGen: C2673759; Orphanet: 90636; OMIM: 220290
- Name:
- Autosomal recessive nonsyndromic hearing loss 1B
- Synonyms:
- Deafness, autosomal recessive 1b
- Identifiers:
- MONDO: MONDO:0012977; MedGen: C2675235; Orphanet: 90636; OMIM: 612645
- Name:
- Autosomal dominant nonsyndromic hearing loss 3B
- Synonyms:
- Deafness, autosomal dominant 3b
- Identifiers:
- MONDO: MONDO:0012975; MedGen: C2675237; Orphanet: 90635; OMIM: 612643
- Name:
- Hidrotic ectodermal dysplasia syndrome (GJB6)
- Synonyms:
- CLOUSTON HIDROTIC ECTODERMAL DYSPLASIA; Ectodermal dysplasia 2, hidrotic; Autosomal dominant hidrotic ectodermal dysplasia; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0007510; MedGen: C0162361; Orphanet: 189; OMIM: 129500; Human Phenotype Ontology: HP:0007529
-
JUNB (1680)
Nucleotide
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Last Updated: Oct 8, 2024