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rs587782750

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 rs587782750(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position68822210
GeneCDH1
is asnp
is mentioned by
dbSNPrs587782750
ebirs587782750
HLIrs587782750
Exacrs587782750
Varsomers587782750
Maprs587782750
PheGenIrs587782750
hapmaprs587782750
1000 genomesrs587782750
hgdprs587782750
ensemblrs587782750
gopubmedrs587782750
geneviewrs587782750
scholarrs587782750
googlers587782750
pharmgkbrs587782750
gwascentralrs587782750
openSNPrs587782750
23andMers587782750
23andMe allrs587782750
SNP Nexus

SNPshotrs587782750
SNPdbers587782750
MSV3drs587782750
GWAS Ctlgrs587782750
Max Magnitude5
ClinVar
Risk rs587782750(T;T)
Alt rs587782750(T;T)
Reference rs587782750(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.68856113C>T
CLNSRC
CLNACC RCV000132257.2,