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rs786202033

From SNPedia

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Geno Mag Summary
(-;C) 5 Hereditary cancer-predisposing syndrome; gastric cancer related?
(C;C) 0 common in clinvar


Make rs786202033(-;-)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position68823461
GeneCDH1
is asnp
is mentioned by
dbSNPrs786202033
ebirs786202033
HLIrs786202033
Exacrs786202033
Varsomers786202033
Maprs786202033
PheGenIrs786202033
hapmaprs786202033
1000 genomesrs786202033
hgdprs786202033
ensemblrs786202033
gopubmedrs786202033
geneviewrs786202033
scholarrs786202033
googlers786202033
pharmgkbrs786202033
gwascentralrs786202033
openSNPrs786202033
23andMers786202033
23andMe allrs786202033
SNP Nexus

SNPshotrs786202033
SNPdbers786202033
MSV3drs786202033
GWAS Ctlgrs786202033
Max Magnitude5

Also known as c.1999delC, the minor allele is considered a pathogenic rare mutation for hereditary diffuse gastric cancer in ClinVar.

ClinVar
Risk rs786202033(;)
Alt rs786202033(;)
Reference rs786202033(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene CDH1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000016.9:g.68857364delC
CLNSRC
CLNACC RCV000164640.1,