NM_003466.4(PAX8):c.*2527A>G AND Hypothyroidism, congenital, nongoitrous, 2
- 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:
- RCV000321557.5
Allele description [Variation Report for NM_003466.4(PAX8):c.*2527A>G]
NM_003466.4(PAX8):c.*2527A>G
Condition(s)
Assertion and evidence details
Last Updated: Apr 9, 2023