Variant (rsID / SNP)

rs2072372

rs2072372 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CD9. Location: chromosome 12, position 6,344,600. The table records no clinical significance for this variant.

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Reference-table entries

CD9Not classified

Variant type: intron_variant
Chromosome / position: 12:6344600
HGVS: NM_001769.4,c.448-42C>A
Allele change: Silent

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.