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rs878854691

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878854691(A;A)
Make rs878854691(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position68737418
GeneCDH1
is asnp
is mentioned by
dbSNPrs878854691
ebirs878854691
HLIrs878854691
Exacrs878854691
Varsomers878854691
Maprs878854691
PheGenIrs878854691
hapmaprs878854691
1000 genomesrs878854691
hgdprs878854691
ensemblrs878854691
gopubmedrs878854691
geneviewrs878854691
scholarrs878854691
googlers878854691
pharmgkbrs878854691
gwascentralrs878854691
openSNPrs878854691
23andMers878854691
23andMe allrs878854691
SNP Nexus

SNPshotrs878854691
SNPdbers878854691
MSV3drs878854691
GWAS Ctlgrs878854691
Max Magnitude0
ClinVar
Risk rs878854691(A;A)
Alt rs878854691(A;A)
Reference rs878854691(G;G)
Significance Probable-Pathogenic
Disease Hereditary diffuse gastric cancer
Variation info
Gene CDH1
CLNDBN Hereditary diffuse gastric cancer
Reversed 0
HGVS NC_000016.9:g.68771321G>A
CLNSRC
CLNACC RCV000230267.1,