Variant (rsID / SNP)

rs3173798

rs3173798 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CD36. Location: chromosome 7, position 80,285,850. Clinical significance in the table: Benign.

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Reference-table entries

CD36Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 7:80285850
Cytoband: 7q21.11
HGVS: NM_001001548.3(CD36):c.121-6T>C
Allele change: Silent

Associated conditions / phenotypes

Platelet-type bleeding disorder 10

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.