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rs202115589

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs202115589(C;C)
Make rs202115589(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position68819424
GeneCDH1
is asnp
is mentioned by
dbSNPrs202115589
dbSNP (old)rs202115589
ClinGenrs202115589
ebirs202115589
HLIrs202115589
Exacrs202115589
Gnomadrs202115589
Varsomers202115589
Maprs202115589
PheGenIrs202115589
Biobankrs202115589
1000 genomesrs202115589
hgdprs202115589
ensemblrs202115589
gopubmedrs202115589
geneviewrs202115589
scholarrs202115589
googlers202115589
pharmgkbrs202115589
gwascentralrs202115589
openSNPrs202115589
23andMers202115589
23andMe allrs202115589
SNP Nexus

SNPshotrs202115589
SNPdbers202115589
MSV3drs202115589
GWAS Ctlgrs202115589
Max Magnitude0
ClinVar
Risk rs202115589(C;C)
Alt rs202115589(C;C)
Reference Rs202115589(T;T)
Significance Probable-non-pathogenic
Disease not specified Hereditary diffuse gastric cancer
Variation info
Gene CDH1
CLNDBN not specified Hereditary diffuse gastric cancer
Reversed 0
HGVS NC_000016.9:g.68853327T>C
CLNSRC
CLNACC RCV000442492.1, RCV000467987.1,