NM_004525.3(LRP2):c.5100C>T (p.Ser1700=) 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:
- RCV000117536.13
Allele description [Variation Report for NM_004525.3(LRP2):c.5100C>T (p.Ser1700=)]
NM_004525.3(LRP2):c.5100C>T (p.Ser1700=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024