Variant (rsID / SNP)

rs72466472

rs72466472 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLDN1. Location: chromosome 3, position 190,039,888. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

CLDN1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:190039888
Cytoband: 3q28
HGVS: NM_021101.5(CLDN1):c.108C>T (p.Ala36=)
Allele change: Synonymous_A36A

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.