Variant (rsID / SNP)

rs5940915

rs5940915 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CPXCR1. The table records no clinical significance for this variant.

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Reference-table entries

CPXCR1Not classified

Variant type: missense_variant
HGVS: NM_001184771.2,c.8A>C,p.Tyr3Ser
Allele change: Missense_Y3S

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.