Variant (rsID / SNP)
rs4304840
rs4304840 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLEC4D. Location: chromosome 12, position 8,667,897. Clinical significance in the table: Benign.
Reference-table entries
CLEC4DBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:8667897
- Cytoband
- 12p13.31
- HGVS
- NM_080387.5(CLEC4D):c.94A>G (p.Ser32Gly)
- Allele change
- Missense_S32G
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.