NM_006516.4(SLC2A1):c.972+20C>G AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 25, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000612454.1
Allele description [Variation Report for NM_006516.4(SLC2A1):c.972+20C>G]
NM_006516.4(SLC2A1):c.972+20C>G
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 28, 2024