Gene entry
LRSAM1
leucine rich repeat and sterile alpha motif containing 1
- Chromosome
- 9
- Cytoband
- 9q33.3-q34.11
- Variants (rsID)
- 16
LRSAM1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9q33.3-q34.11). Its official name is “leucine rich repeat and sterile alpha motif containing 1”. The reference table lists 16 variants (rsID) for this gene.
Clinically classified variants
10 reference-table entries with clinical significance.
- rs140786088Benignsingle nucleotide variantCharcot-Marie-Tooth disease axonal type 2P
- rs1539567Benignsingle nucleotide variantCharcot-Marie-Tooth disease axonal type 2P|Charcot-Marie-Tooth disease
- rs117692127Conflicting interpretationssingle nucleotide variantCharcot-Marie-Tooth disease axonal type 2P|Charcot-Marie-Tooth disease
- rs367599324Conflicting interpretationssingle nucleotide variant
- rs369353985Conflicting interpretationssingle nucleotide variant
- rs760403428Conflicting interpretationssingle nucleotide variantCharcot-Marie-Tooth disease axonal type 2P
- rs886063456Conflicting interpretationssingle nucleotide variantCharcot-Marie-Tooth disease type 2|Charcot-Marie-Tooth disease axonal type 2P
- rs145382004Likely benignsingle nucleotide variantCharcot-Marie-Tooth disease axonal type 2P
- rs201808404Likely benignsingle nucleotide variantCharcot-Marie-Tooth disease axonal type 2P|Charcot-Marie-Tooth disease
- rs138830549Uncertain significancesingle nucleotide variantCharcot-Marie-Tooth disease axonal type 2P
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.