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rs587781919

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587781919(A;A)
Make rs587781919(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position68801894
GeneCDH1
is asnp
is mentioned by
dbSNPrs587781919
ebirs587781919
HLIrs587781919
Exacrs587781919
Varsomers587781919
Maprs587781919
PheGenIrs587781919
hapmaprs587781919
1000 genomesrs587781919
hgdprs587781919
ensemblrs587781919
gopubmedrs587781919
geneviewrs587781919
scholarrs587781919
googlers587781919
pharmgkbrs587781919
gwascentralrs587781919
openSNPrs587781919
23andMers587781919
23andMe allrs587781919
SNP Nexus

SNPshotrs587781919
SNPdbers587781919
MSV3drs587781919
GWAS Ctlgrs587781919
Max Magnitude0
ClinVar
Risk rs587781919(A;A)
Alt rs587781919(A;A)
Reference rs587781919(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene CDH1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000016.9:g.68835797G>A
CLNSRC
CLNACC RCV000130267.3,