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rs876658865

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CCC;CCC) 0 common in clinvar
Chromosome16
Position68738372
GeneCDH1
is asnp
is mentioned by
dbSNPrs876658865
dbSNP (old)rs876658865
ClinGenrs876658865
ebirs876658865
HLIrs876658865
Exacrs876658865
Gnomadrs876658865
Varsomers876658865
Maprs876658865
PheGenIrs876658865
Biobankrs876658865
1000 genomesrs876658865
hgdprs876658865
ensemblrs876658865
gopubmedrs876658865
geneviewrs876658865
scholarrs876658865
googlers876658865
pharmgkbrs876658865
gwascentralrs876658865
openSNPrs876658865
23andMers876658865
23andMe allrs876658865
SNP Nexus

SNPshotrs876658865
SNPdbers876658865
MSV3drs876658865
GWAS Ctlgrs876658865
Max Magnitude0
ClinVar
Risk rs876658865(T;T)
Alt rs876658865(T;T)
Reference Rs876658865(CCC;CCC)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene CDH1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000016.9:g.68772275_68772277delCCCinsT
CLNSRC
CLNACC RCV000215517.1,