Variant (rsID / SNP)
rs3211938
rs3211938 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CD36. Location: chromosome 7, position 80,300,449. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
CD36Conflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:80300449
- Cytoband
- 7q21.11
- HGVS
- NM_001001548.3(CD36):c.975T>G (p.Tyr325Ter)
- Allele change
- Nonsense_Y325X
Associated conditions / phenotypes
Platelet-type bleeding disorder 10|Malaria, cerebral, susceptibility to
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.