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rs587780537

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 rs587780537(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position68810224
GeneCDH1
is asnp
is mentioned by
dbSNPrs587780537
ebirs587780537
HLIrs587780537
Exacrs587780537
Varsomers587780537
Maprs587780537
PheGenIrs587780537
hapmaprs587780537
1000 genomesrs587780537
hgdprs587780537
ensemblrs587780537
gopubmedrs587780537
geneviewrs587780537
scholarrs587780537
googlers587780537
pharmgkbrs587780537
gwascentralrs587780537
openSNPrs587780537
23andMers587780537
23andMe allrs587780537
SNP Nexus

SNPshotrs587780537
SNPdbers587780537
MSV3drs587780537
GWAS Ctlgrs587780537
Max Magnitude5
ClinVar
Risk rs587780537(A;A)
Alt rs587780537(A;A)
Reference rs587780537(G;G)
Significance Pathogenic
Disease Hereditary diffuse gastric cancer Hereditary cancer-predisposing syndrome not specified Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene CDH1
CLNDBN Hereditary diffuse gastric cancer Hereditary cancer-predisposing syndrome not specified Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000016.9:g.68844127G>A
CLNSRC
CLNACC RCV000119150.3, RCV000160387.3, RCV000212355.1, RCV000222484.1,