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rs587782677

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587782677(C;G)
Make rs587782677(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position68801859
GeneCDH1
is asnp
is mentioned by
dbSNPrs587782677
ebirs587782677
HLIrs587782677
Exacrs587782677
Varsomers587782677
Maprs587782677
PheGenIrs587782677
hapmaprs587782677
1000 genomesrs587782677
hgdprs587782677
ensemblrs587782677
gopubmedrs587782677
geneviewrs587782677
scholarrs587782677
googlers587782677
pharmgkbrs587782677
gwascentralrs587782677
openSNPrs587782677
23andMers587782677
23andMe allrs587782677
SNP Nexus

SNPshotrs587782677
SNPdbers587782677
MSV3drs587782677
GWAS Ctlgrs587782677
Max Magnitude0
ClinVar
Risk rs587782677(G;G)
Alt rs587782677(G;G)
Reference rs587782677(C;C)
Significance Unknown
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene CDH1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000016.9:g.68835762C>G
CLNSRC
CLNACC RCV000132103.2,