Variant (rsID / SNP)
rs149132399
rs149132399 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CAPN5. Location: chromosome 11, position 76,795,984. Clinical significance in the table: Likely benign.
Reference-table entries
CAPN5Likely benign
- Clinical significance (as recorded)
- Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:76795984
- Cytoband
- 11q13.5
- HGVS
- NM_004055.5(CAPN5):c.52C>T (p.Arg18Trp)
- Allele change
- Missense_R18W
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.