Have questions? Visit https://www.reddit.com/r/SNPedia

rs121964873

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 6.7 CDH1-based gastric cancer risk
Make rs121964873(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position68810290
GeneCDH1
is asnp
is mentioned by
dbSNPrs121964873
dbSNP (classic)rs121964873
ClinGenrs121964873
ebirs121964873
HLIrs121964873
Exacrs121964873
Gnomadrs121964873
Varsomers121964873
LitVarrs121964873
Maprs121964873
PheGenIrs121964873
Biobankrs121964873
1000 genomesrs121964873
hgdprs121964873
ensemblrs121964873
geneviewrs121964873
scholarrs121964873
googlers121964873
pharmgkbrs121964873
gwascentralrs121964873
openSNPrs121964873
23andMers121964873
SNPshotrs121964873
SNPdbers121964873
MSV3drs121964873
GWAS Ctlgrs121964873
Max Magnitude6.7
OMIM192090
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121964873(A;A) rs121964873(T;T)
Alt rs121964873(A;A) rs121964873(T;T)
Reference Rs121964873(G;G)
Significance Pathogenic
Disease Hereditary diffuse gastric cancer not specified Breast cancer
Variation info
Gene CDH1
CLNDBN Hereditary diffuse gastric cancer not specified Breast cancer, lobular
Reversed 0
HGVS NC_000016.9:g.68844193G>A; NC_000016.9:g.68844193G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000475944.1, RCV000480274.1, RCV000013021.5,