Variant (rsID / SNP)

rs75326924

rs75326924 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CD36. Location: chromosome 7, position 80,286,003. Clinical significance in the table: Pathogenic.

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Reference-table entries

CD36Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 7:80286003
Cytoband: 7q21.11
HGVS: NM_001001548.3(CD36):c.268C>T (p.Pro90Ser)
Allele change: Missense_P90S

Associated conditions / phenotypes

Platelet-type bleeding disorder 10|Inherited bleeding disorder, platelet-type

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.