NM_000199.3(SGSH):c.-145G>A AND not provided
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Jun 19, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000829194.11
Allele description [Variation Report for NM_000199.3(SGSH):c.-145G>A]
NM_000199.3(SGSH):c.-145G>A
Condition(s)
- Synonyms:
- none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Nov 30, 2024