Variant (rsID / SNP)
rs3769824
rs3769824 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CASP8. Location: chromosome 2, position 202,122,956. Clinical significance in the table: Benign.
Reference-table entries
CASP8Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:202122956
- Cytoband
- 2q33.1
- HGVS
- NM_001228.4(CASP8):c.-26-8228T>C
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.