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rs878854697

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878854697(G;T)
Make rs878854697(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position68810342
GeneCDH1
is asnp
is mentioned by
dbSNPrs878854697
ebirs878854697
HLIrs878854697
Exacrs878854697
Varsomers878854697
Maprs878854697
PheGenIrs878854697
hapmaprs878854697
1000 genomesrs878854697
hgdprs878854697
ensemblrs878854697
gopubmedrs878854697
geneviewrs878854697
scholarrs878854697
googlers878854697
pharmgkbrs878854697
gwascentralrs878854697
openSNPrs878854697
23andMers878854697
23andMe allrs878854697
SNP Nexus

SNPshotrs878854697
SNPdbers878854697
MSV3drs878854697
GWAS Ctlgrs878854697
Max Magnitude0
ClinVar
Risk rs878854697(T;T)
Alt rs878854697(T;T)
Reference rs878854697(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.68844245G>T
CLNSRC
CLNACC RCV000229653.1,