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rs1801026

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1801026(C;T)
Make rs1801026(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position68833553
GeneCDH1
is asnp
is mentioned by
dbSNPrs1801026
dbSNP (old)rs1801026
ClinGenrs1801026
ebirs1801026
HLIrs1801026
Exacrs1801026
Gnomadrs1801026
Varsomers1801026
Maprs1801026
PheGenIrs1801026
Biobankrs1801026
1000 genomesrs1801026
hgdprs1801026
ensemblrs1801026
gopubmedrs1801026
geneviewrs1801026
scholarrs1801026
googlers1801026
pharmgkbrs1801026
gwascentralrs1801026
openSNPrs1801026
23andMers1801026
23andMe allrs1801026
SNP Nexus

SNPshotrs1801026
SNPdbers1801026
MSV3drs1801026
GWAS Ctlgrs1801026
Max Magnitude0

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

[PMID 27852262OA-icon.png] E-cadherin genetic variants predict survival outcome in breast cancer patients.

ClinVar
Risk rs1801026(A;A) rs1801026(G;G) rs1801026(T;T)
Alt rs1801026(A;A) rs1801026(G;G) rs1801026(T;T)
Reference Rs1801026(C;C)
Significance Non-pathogenic
Disease Hereditary diffuse gastric cancer
Variation info
Gene CDH1
CLNDBN Hereditary diffuse gastric cancer
Reversed 0
HGVS NC_000016.9:g.68867456C>T
CLNSRC
CLNACC RCV000325599.1,