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Variant (rsID / SNP)

rs4562

CLDN7

rs4562 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLDN7. Location: chromosome 17, position 7,163,739. The table records no clinical significance for this variant.

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Reference-table entries

CLDN7Not classified
Variant type
missense_variant
Chromosome / position
17:7163739
HGVS
NM_001185022.2,c.590T>C,p.Val197Ala
Allele change
Silent

Associated conditions / phenotypes

Breast Cancer|Colorectal Cancer

Public references

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