NM_006446.5(SLCO1B1):c.571T>C (p.Leu191=) AND not specified
- Germline classification:
- Benign (2 submissions)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000243891.10
Allele description [Variation Report for NM_006446.5(SLCO1B1):c.571T>C (p.Leu191=)]
NM_006446.5(SLCO1B1):c.571T>C (p.Leu191=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 16, 2024