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rs1801552

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1801552(C;C)
Make rs1801552(C;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position68823538
GeneCDH1
is asnp
is mentioned by
dbSNPrs1801552
ebirs1801552
HLIrs1801552
Exacrs1801552
Varsomers1801552
Maprs1801552
PheGenIrs1801552
hapmaprs1801552
1000 genomesrs1801552
hgdprs1801552
ensemblrs1801552
gopubmedrs1801552
geneviewrs1801552
scholarrs1801552
googlers1801552
pharmgkbrs1801552
gwascentralrs1801552
openSNPrs1801552
23andMers1801552
23andMe allrs1801552
SNP Nexus

SNPshotrs1801552
SNPdbers1801552
MSV3drs1801552
GWAS Ctlgrs1801552
GMAF0.3067
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 22535324] CDH1 gene polymorphisms, plasma CDH1 levels and risk of gastric cancer in a Chinese population


[PMID 24838934OA-icon.png] Nucleotide variants of the cancer predisposing gene CDH1 and the risk of non-syndromic cleft lip with or without cleft palate


[PMID 25150394] Genetic variation of the E-cadherin gene is associated with primary infertility in patients with ovarian endometriosis


ClinVar
Risk rs1801552(C;C)
Alt rs1801552(C;C)
Reference rs1801552(T;T)
Significance Non-pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene CDH1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000016.9:g.68857441T>C
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000132164.2,