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rs121964871

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121964871(C;G)
Make rs121964871(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position68823593
GeneCDH1
is asnp
is mentioned by
dbSNPrs121964871
ebirs121964871
HLIrs121964871
Exacrs121964871
Varsomers121964871
Maprs121964871
PheGenIrs121964871
hapmaprs121964871
1000 genomesrs121964871
hgdprs121964871
ensemblrs121964871
gopubmedrs121964871
geneviewrs121964871
scholarrs121964871
googlers121964871
pharmgkbrs121964871
gwascentralrs121964871
openSNPrs121964871
23andMers121964871
23andMe allrs121964871
SNP Nexus

SNPshotrs121964871
SNPdbers121964871
MSV3drs121964871
GWAS Ctlgrs121964871
Max Magnitude0
OMIM192090
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121964871(G;G)
Alt rs121964871(G;G)
Reference rs121964871(C;C)
Significance Pathogenic
Disease Endometrial carcinoma Hereditary cancer-predisposing syndrome Hereditary diffuse gastric cancer
Variation info
Gene CDH1
CLNDBN Endometrial carcinoma Hereditary cancer-predisposing syndrome Hereditary diffuse gastric cancer
Reversed 0
HGVS NC_000016.9:g.68857496C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000013017.4, RCV000130551.2, RCV000196099.2,