Variant (rsID / SNP)

rs200067322

rs200067322 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CD36. Location: chromosome 7, position 80,293,761. Clinical significance in the table: Uncertain significance.

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Reference-table entries

CD36Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 7:80293761
Cytoband: 7q21.11
HGVS: NM_001001548.3(CD36):c.649G>A (p.Gly217Arg)
Allele change: Missense_G217R

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.