Gene entry
EFNB1
ephrin B1
- Chromosome
- X
- Cytoband
- Xq13.1
- Variants (rsID)
- 12
EFNB1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xq13.1). Its official name is “ephrin B1”. The reference table lists 12 variants (rsID) for this gene.
Clinically classified variants
8 reference-table entries with clinical significance.
- rs104894796Pathogenicsingle nucleotide variantCraniofrontonasal syndrome
- rs104894801Pathogenicsingle nucleotide variantCraniofrontonasal syndrome
- rs104894802Pathogenicsingle nucleotide variantCraniofrontonasal syndrome
- rs104894803Pathogenicsingle nucleotide variantCraniofrontonasal syndrome
- rs104894804Pathogenicsingle nucleotide variantCraniofrontonasal syndrome
- rs28935170Pathogenicsingle nucleotide variantCraniofrontonasal syndrome
- rs28936070Pathogenicsingle nucleotide variantCraniofrontonasal syndrome
- rs28936071Pathogenicsingle nucleotide variantCraniofrontonasal syndrome
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.