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rs587781276

From SNPedia

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Geno Mag Summary
(-;TG) 5 Hereditary cancer-predisposing syndrome; gastric cancer related?
(TG;TG) 0 common in clinvar


Make rs587781276(-;-)
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position68823526
GeneCDH1
is asnp
is mentioned by
dbSNPrs587781276
ebirs587781276
HLIrs587781276
Exacrs587781276
Varsomers587781276
Maprs587781276
PheGenIrs587781276
hapmaprs587781276
1000 genomesrs587781276
hgdprs587781276
ensemblrs587781276
gopubmedrs587781276
geneviewrs587781276
scholarrs587781276
googlers587781276
pharmgkbrs587781276
gwascentralrs587781276
openSNPrs587781276
23andMers587781276
23andMe allrs587781276
SNP Nexus

SNPshotrs587781276
SNPdbers587781276
MSV3drs587781276
GWAS Ctlgrs587781276
Max Magnitude5

Also known as c.2064_2065delTG, the minor allele is considered a pathogenic rare mutation for hereditary diffuse gastric cancer in ClinVar.

ClinVar
Risk rs587781276(;)
Alt rs587781276(;)
Reference rs587781276(TG;TG)
Significance 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.68857429_68857430delTG
CLNSRC
CLNACC RCV000128928.2, RCV000168178.1,