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

rs869312764

From SNPedia

Merged intors863224505
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869312764(-;-)
Make rs869312764(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position68812190
GeneCDH1
is asnp
is mentioned by
dbSNPrs869312764
dbSNP (old)rs869312764
ClinGenrs869312764
ebirs869312764
HLIrs869312764
Exacrs869312764
Gnomadrs869312764
Varsomers869312764
Maprs869312764
PheGenIrs869312764
Biobankrs869312764
1000 genomesrs869312764
hgdprs869312764
ensemblrs869312764
gopubmedrs869312764
geneviewrs869312764
scholarrs869312764
googlers869312764
pharmgkbrs869312764
gwascentralrs869312764
openSNPrs869312764
23andMers869312764
23andMe allrs869312764
SNP Nexus

SNPshotrs869312764
SNPdbers869312764
MSV3drs869312764
GWAS Ctlgrs869312764
StatusMerged into rs863224505
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs869312764(T;T)
Significance Pathogenic
Disease Hereditary diffuse gastric cancer Hereditary cancer-predisposing syndrome
Variation info
Gene CDH1
CLNDBN Hereditary diffuse gastric cancer Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000016.9:g.68846093delT
CLNSRC
CLNACC RCV000196464.1, RCV000210107.1,