NM_001044385.3(TMEM237):c.75-6T>C AND not specified
- Germline classification:
- Benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000241620.5
Allele description [Variation Report for NM_001044385.3(TMEM237):c.75-6T>C]
NM_001044385.3(TMEM237):c.75-6T>C
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 10, 2024