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rs864622655

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;A) 5 Hereditary cancer-predisposing syndrome; gastric cancer related?


Make rs864622655(-;-)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position68808540
GeneCDH1
is asnp
is mentioned by
dbSNPrs864622655
ebirs864622655
HLIrs864622655
Exacrs864622655
Varsomers864622655
Maprs864622655
PheGenIrs864622655
hapmaprs864622655
1000 genomesrs864622655
hgdprs864622655
ensemblrs864622655
gopubmedrs864622655
geneviewrs864622655
scholarrs864622655
googlers864622655
pharmgkbrs864622655
gwascentralrs864622655
openSNPrs864622655
23andMers864622655
23andMe allrs864622655
SNP Nexus

SNPshotrs864622655
SNPdbers864622655
MSV3drs864622655
GWAS Ctlgrs864622655
Max Magnitude5

Also known as c.504delA, the minor allele is considered a pathogenic rare mutation for hereditary diffuse gastric cancer in ClinVar.

ClinVar
Risk rs864622655(;)
Alt rs864622655(;)
Reference rs864622655(A;A)
Significance Pathogenic
Disease Hereditary diffuse gastric cancer
Variation info
Gene CDH1
CLNDBN Hereditary diffuse gastric cancer
Reversed 0
HGVS NC_000016.9:g.68842443delA
CLNSRC
CLNACC RCV000204728.2,