Variant (rsID / SNP)
rs6555888
rs6555888 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FOXI1. Location: chromosome 5, position 169,536,150. Clinical significance in the table: Benign.
Reference-table entries
FOXI1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 5:169536150
- Cytoband
- 5q35.1
- HGVS
- NM_012188.5(FOXI1):c.*535A>G
- Allele change
- Silent
Associated conditions / phenotypes
Autosomal recessive nonsyndromic hearing loss 4
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.