Variant (rsID / SNP)
rs11651675
rs11651675 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMC8. Location: chromosome 17, position 76,134,237. Clinical significance in the table: Benign.
Reference-table entries
TMC8Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 17:76134237
- Cytoband
- 17q25.3
- HGVS
- NM_152468.5(TMC8):c.1501G>A (p.Val501Ile)
- Allele change
- Missense_V501I
Associated conditions / phenotypes
Epidermodysplasia verruciformis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.