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rs587781290

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587781290(-;-)
Make rs587781290(-;A)
Make rs587781290(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position68808557
GeneCDH1
is asnp
is mentioned by
dbSNPrs587781290
ebirs587781290
HLIrs587781290
Exacrs587781290
Varsomers587781290
Maprs587781290
PheGenIrs587781290
hapmaprs587781290
1000 genomesrs587781290
hgdprs587781290
ensemblrs587781290
gopubmedrs587781290
geneviewrs587781290
scholarrs587781290
googlers587781290
pharmgkbrs587781290
gwascentralrs587781290
openSNPrs587781290
23andMers587781290
23andMe allrs587781290
SNP Nexus

SNPshotrs587781290
SNPdbers587781290
MSV3drs587781290
GWAS Ctlgrs587781290
Max Magnitude0
ClinVar
Risk rs587781290(A;A)
Alt rs587781290(A;A)
Reference rs587781290(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene CDH1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000016.9:g.68842460dupA
CLNSRC
CLNACC RCV000128977.2,