Variant (rsID / SNP)

rs5934731

rs5934731 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLDN34. The table records no clinical significance for this variant.

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Reference-table entries

CLDN34Not classified

Variant type: synonymous_variant
HGVS: NM_001195081.2,c.447C>T,p.Tyr149Tyr
Allele change: Synonymous_Y149Y

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.