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rs587781335

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587781335(C;G)
Make rs587781335(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position68829754
GeneCDH1
is asnp
is mentioned by
dbSNPrs587781335
ebirs587781335
HLIrs587781335
Exacrs587781335
Varsomers587781335
Maprs587781335
PheGenIrs587781335
hapmaprs587781335
1000 genomesrs587781335
hgdprs587781335
ensemblrs587781335
gopubmedrs587781335
geneviewrs587781335
scholarrs587781335
googlers587781335
pharmgkbrs587781335
gwascentralrs587781335
openSNPrs587781335
23andMers587781335
23andMe allrs587781335
SNP Nexus

SNPshotrs587781335
SNPdbers587781335
MSV3drs587781335
GWAS Ctlgrs587781335
Max Magnitude0
ClinVar
Risk rs587781335(G;G)
Alt rs587781335(G;G)
Reference rs587781335(C;C)
Significance Unknown
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.68863657C>G
CLNSRC
CLNACC RCV000129091.2, RCV000167901.1,