Variant (rsID / SNP)
rs58232698
rs58232698 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TBC1D4. Location: chromosome 13, position 75,866,368. Clinical significance in the table: Benign.
Reference-table entries
TBC1D4Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 13:75866368
- Cytoband
- 13q22.2
- HGVS
- NM_014832.5(TBC1D4):c.3356T>C (p.Val1119Ala)
- Allele change
- Missense_V1119A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.