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rs587782359

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 5 Hereditary cancer-predisposing syndrome; gastric cancer related?
Make rs587782359(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position68812244
GeneCDH1
is asnp
is mentioned by
dbSNPrs587782359
ebirs587782359
HLIrs587782359
Exacrs587782359
Varsomers587782359
Maprs587782359
PheGenIrs587782359
hapmaprs587782359
1000 genomesrs587782359
hgdprs587782359
ensemblrs587782359
gopubmedrs587782359
geneviewrs587782359
scholarrs587782359
googlers587782359
pharmgkbrs587782359
gwascentralrs587782359
openSNPrs587782359
23andMers587782359
23andMe allrs587782359
SNP Nexus

SNPshotrs587782359
SNPdbers587782359
MSV3drs587782359
GWAS Ctlgrs587782359
Max Magnitude5
ClinVar
Risk rs587782359(T;T)
Alt rs587782359(T;T)
Reference rs587782359(C;C)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome Hereditary diffuse gastric cancer
Variation info
Gene CDH1
CLNDBN Hereditary cancer-predisposing syndrome Hereditary diffuse gastric cancer
Reversed 0
HGVS NC_000016.9:g.68846147C>T
CLNSRC
CLNACC RCV000131314.2, RCV000231218.1,