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rs878854690

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;G) 5 Hereditary diffuse gastric cancer
Make rs878854690(-;-)
Make rs878854690(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position68801866
GeneCDH1
is asnp
is mentioned by
dbSNPrs878854690
ebirs878854690
HLIrs878854690
Exacrs878854690
Varsomers878854690
Maprs878854690
PheGenIrs878854690
hapmaprs878854690
1000 genomesrs878854690
hgdprs878854690
ensemblrs878854690
gopubmedrs878854690
geneviewrs878854690
scholarrs878854690
googlers878854690
pharmgkbrs878854690
gwascentralrs878854690
openSNPrs878854690
23andMers878854690
23andMe allrs878854690
SNP Nexus

SNPshotrs878854690
SNPdbers878854690
MSV3drs878854690
GWAS Ctlgrs878854690
Max Magnitude5

Also known as c.360dupG, the minor allele is considered a pathogenic rare mutation for hereditary diffuse gastric cancer in ClinVar.

ClinVar
Risk rs878854690(G;G)
Alt rs878854690(G;G)
Reference rs878854690(;)
Significance Pathogenic
Disease Hereditary diffuse gastric cancer
Variation info
Gene CDH1
CLNDBN Hereditary diffuse gastric cancer
Reversed 0
HGVS NC_000016.9:g.68835769dupG
CLNSRC
CLNACC RCV000227876.1,