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rs786204165

From SNPedia

Merged intors587781276
Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs786204165(-;-)
Make rs786204165(-;TG)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position68823524
GeneCDH1
is asnp
is mentioned by
dbSNPrs786204165
dbSNP (old)rs786204165
ClinGenrs786204165
ebirs786204165
HLIrs786204165
Exacrs786204165
Gnomadrs786204165
Varsomers786204165
Maprs786204165
PheGenIrs786204165
Biobankrs786204165
1000 genomesrs786204165
hgdprs786204165
ensemblrs786204165
gopubmedrs786204165
geneviewrs786204165
scholarrs786204165
googlers786204165
pharmgkbrs786204165
gwascentralrs786204165
openSNPrs786204165
23andMers786204165
23andMe allrs786204165
SNP Nexus

SNPshotrs786204165
SNPdbers786204165
MSV3drs786204165
GWAS Ctlgrs786204165
StatusMerged into rs587781276
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs786204165(TG;TG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Hereditary diffuse gastric cancer
Variation info
Gene CDH1
CLNDBN Hereditary cancer-predisposing syndrome Hereditary diffuse gastric cancer
Reversed 0
HGVS NC_000016.9:g.68857429_68857430delTG
CLNSRC
CLNACC RCV000128928.2, RCV000168178.1,