NM_000243.3(MEFV):c.1759+8C>T AND not specified
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Nov 19, 2014
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000180116.15
Allele description [Variation Report for NM_000243.3(MEFV):c.1759+8C>T]
NM_000243.3(MEFV):c.1759+8C>T
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
eggc.vipDSH (0)
BioProject
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Last Updated: Jun 2, 2024