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rs587782798

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 rs587782798(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position68813322
GeneCDH1
is asnp
is mentioned by
dbSNPrs587782798
ebirs587782798
HLIrs587782798
Exacrs587782798
Varsomers587782798
Maprs587782798
PheGenIrs587782798
hapmaprs587782798
1000 genomesrs587782798
hgdprs587782798
ensemblrs587782798
gopubmedrs587782798
geneviewrs587782798
scholarrs587782798
googlers587782798
pharmgkbrs587782798
gwascentralrs587782798
openSNPrs587782798
23andMers587782798
23andMe allrs587782798
SNP Nexus

SNPshotrs587782798
SNPdbers587782798
MSV3drs587782798
GWAS Ctlgrs587782798
Max Magnitude5
ClinVar
Risk rs587782798(T;T)
Alt rs587782798(T;T)
Reference rs587782798(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene CDH1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000016.9:g.68847225C>T
CLNSRC
CLNACC RCV000132351.2,