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

rs876659503

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876659503(C;C)
Make rs876659503(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position68810302
GeneCDH1
is asnp
is mentioned by
dbSNPrs876659503
dbSNP (classic)rs876659503
ClinGenrs876659503
ebirs876659503
HLIrs876659503
Exacrs876659503
Gnomadrs876659503
Varsomers876659503
LitVarrs876659503
Maprs876659503
PheGenIrs876659503
Biobankrs876659503
1000 genomesrs876659503
hgdprs876659503
ensemblrs876659503
geneviewrs876659503
scholarrs876659503
googlers876659503
pharmgkbrs876659503
gwascentralrs876659503
openSNPrs876659503
23andMers876659503
SNPshotrs876659503
SNPdbers876659503
MSV3drs876659503
GWAS Ctlgrs876659503
Max Magnitude0
ClinVar
Risk rs876659503(C;C) rs876659503(T;T)
Alt rs876659503(C;C) rs876659503(T;T)
Reference Rs876659503(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Hereditary diffuse gastric cancer not specified
Variation info
Gene CDH1
CLNDBN Hereditary cancer-predisposing syndrome Hereditary diffuse gastric cancer not specified
Reversed 0
HGVS NC_000016.9:g.68844205G>C; NC_000016.9:g.68844205G>T
CLNSRC
CLNACC RCV000217330.1, RCV000465251.1, RCV000483098.1, RCV000457462.1,