Gene entry
LHFPL5
LHFPL tetraspan subfamily member 5
- Chromosome
- 6
- Cytoband
- 6p21.31
- Variants (rsID)
- 7
LHFPL5 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6p21.31). Its official name is “LHFPL tetraspan subfamily member 5”. The reference table lists 7 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs149941106Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 67
- rs104893975Pathogenicsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 67
- rs104893976Pathogenicsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 67
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.