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rs587783050

From SNPedia

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


Make rs587783050(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position68812263
GeneCDH1
is asnp
is mentioned by
dbSNPrs587783050
ebirs587783050
HLIrs587783050
Exacrs587783050
Varsomers587783050
Maprs587783050
PheGenIrs587783050
hapmaprs587783050
1000 genomesrs587783050
hgdprs587783050
ensemblrs587783050
gopubmedrs587783050
geneviewrs587783050
scholarrs587783050
googlers587783050
pharmgkbrs587783050
gwascentralrs587783050
openSNPrs587783050
23andMers587783050
23andMe allrs587783050
SNP Nexus

SNPshotrs587783050
SNPdbers587783050
MSV3drs587783050
GWAS Ctlgrs587783050
Max Magnitude5

Also known as c.1137G>A, the minor allele is considered a pathogenic rare mutation for hereditary diffuse gastric cancer in ClinVar.

ClinVar
Risk rs587783050(A;A)
Alt rs587783050(A;A)
Reference rs587783050(G;G)
Significance Pathogenic
Disease Hereditary diffuse gastric cancer Hereditary cancer-predisposing syndrome
Variation info
Gene CDH1
CLNDBN Hereditary diffuse gastric cancer Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000016.9:g.68846166G>A
CLNSRC
CLNACC RCV000144593.1, RCV000162417.1,