Gene entry
SEMA4A
semaphorin 4A
- Chromosome
- 1
- Cytoband
- 1q22
- Variants (rsID)
- 9
SEMA4A is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1q22). Its official name is “semaphorin 4A”. The reference table lists 9 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs41265017Benignsingle nucleotide variantRetinitis pigmentosa 35|Cone-rod dystrophy 10|Retinitis Pigmentosa, Recessive|Retinitis pigmentosa
- rs76381440Benignsingle nucleotide variantRetinitis pigmentosa|Cone-rod dystrophy 10
- rs149711133Conflicting interpretationssingle nucleotide variantRetinitis Pigmentosa, Recessive|Cone-rod dystrophy 10|Retinitis pigmentosa
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.