NM_006440.5(TXNRD2):c.374+13C>T AND not specified
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Oct 4, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000428772.2
Allele description [Variation Report for NM_006440.5(TXNRD2):c.374+13C>T]
NM_006440.5(TXNRD2):c.374+13C>T
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
29869[HGNC] (101)
ClinVar
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See more...Assertion and evidence details
Last Updated: Apr 6, 2024