NM_170682.4(P2RX2):c.1325_1335del (p.Ile441_Ser442insTer) AND Autosomal dominant nonsyndromic hearing loss 41
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 7, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002500690.1
Allele description [Variation Report for NM_170682.4(P2RX2):c.1325_1335del (p.Ile441_Ser442insTer)]
NM_170682.4(P2RX2):c.1325_1335del (p.Ile441_Ser442insTer)
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024