NM_139319.3(SLC17A8):c.-32T>G AND Autosomal dominant nonsyndromic hearing loss 25
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000396555.5
Allele description [Variation Report for NM_139319.3(SLC17A8):c.-32T>G]
NM_139319.3(SLC17A8):c.-32T>G
Condition(s)
Assertion and evidence details
Last Updated: Apr 9, 2023