Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs33935154

CDH1

rs33935154 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDH1. Location: chromosome 16, position 68,856,041. Clinical significance in the table: Benign.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

CDH1Benign
Clinical significance (as recorded)
Benign
Variant type
single nucleotide variant
Chromosome / position
16:68856041
Cytoband
16q22.1
HGVS
NM_004360.5(CDH1):c.1849G>A (p.Ala617Thr)
Allele change
Missense_A617T

Associated conditions / phenotypes

Endometrial carcinoma|Hereditary diffuse gastric adenocarcinoma|Hereditary cancer-predisposing syndrome|Malignant tumor of breast|Breast and/or ovarian cancer

Public references

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