NM_000369.5(TSHR):c.881+3A>G AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 19, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000202706.1
Allele description [Variation Report for NM_000369.5(TSHR):c.881+3A>G]
NM_000369.5(TSHR):c.881+3A>G
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 16, 2024