Variant (rsID / SNP)

rs74026937

rs74026937 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDH3. Location: chromosome 16, position 68,716,295. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

CDH3Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 16:68716295
Cytoband: 16q22.1
HGVS: NM_001793.6(CDH3):c.1087C>T (p.Arg363Cys)
Allele change: Missense_R363C

Associated conditions / phenotypes

EEM syndrome

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.