NM_001171.6(ABCC6):c.4002G>C (p.Gly1334=) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Dec 14, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000487735.22
Allele description [Variation Report for NM_001171.6(ABCC6):c.4002G>C (p.Gly1334=)]
NM_001171.6(ABCC6):c.4002G>C (p.Gly1334=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 10, 2024