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rs13689

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs13689(C;C)
Make rs13689(C;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position68834619
GeneCDH1
is asnp
is mentioned by
dbSNPrs13689
dbSNP (old)rs13689
ClinGenrs13689
ebirs13689
HLIrs13689
Exacrs13689
Gnomadrs13689
Varsomers13689
Maprs13689
PheGenIrs13689
Biobankrs13689
1000 genomesrs13689
hgdprs13689
ensemblrs13689
gopubmedrs13689
geneviewrs13689
scholarrs13689
googlers13689
pharmgkbrs13689
gwascentralrs13689
openSNPrs13689
23andMers13689
23andMe allrs13689
SNP Nexus

SNPshotrs13689
SNPdbers13689
MSV3drs13689
GWAS Ctlgrs13689
GMAF0.1731
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 22330421] E-cadherin polymorphisms and susceptibility to arsenic-related skin lesions in West Bengal, India.


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

ClinVar
Risk rs13689(A;A) rs13689(C;C) rs13689(G;G)
Alt rs13689(A;A) rs13689(C;C) rs13689(G;G)
Reference Rs13689(T;T)
Significance Non-pathogenic
Disease Hereditary diffuse gastric cancer
Variation info
Gene CDH1
CLNDBN Hereditary diffuse gastric cancer
Reversed 0
HGVS NC_000016.9:g.68868522T>C
CLNSRC
CLNACC RCV000375550.1,