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rs869312765

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312765(-;-)
Make rs869312765(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position68815699
GeneCDH1
is asnp
is mentioned by
dbSNPrs869312765
ebirs869312765
HLIrs869312765
Exacrs869312765
Varsomers869312765
Maprs869312765
PheGenIrs869312765
hapmaprs869312765
1000 genomesrs869312765
hgdprs869312765
ensemblrs869312765
gopubmedrs869312765
geneviewrs869312765
scholarrs869312765
googlers869312765
pharmgkbrs869312765
gwascentralrs869312765
openSNPrs869312765
23andMers869312765
23andMe allrs869312765
SNP Nexus

SNPshotrs869312765
SNPdbers869312765
MSV3drs869312765
GWAS Ctlgrs869312765
Max Magnitude0
ClinVar
Risk rs869312765(;)
Alt rs869312765(;)
Reference rs869312765(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene CDH1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000016.9:g.68849602delG
CLNSRC
CLNACC RCV000210159.1,