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rs771085839

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs771085839(C;C)
Make rs771085839(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position68808692
GeneCDH1
is asnp
is mentioned by
dbSNPrs771085839
dbSNP (classic)rs771085839
ClinGenrs771085839
ebirs771085839
HLIrs771085839
Exacrs771085839
Gnomadrs771085839
Varsomers771085839
LitVarrs771085839
Maprs771085839
PheGenIrs771085839
Biobankrs771085839
1000 genomesrs771085839
hgdprs771085839
ensemblrs771085839
geneviewrs771085839
scholarrs771085839
googlers771085839
pharmgkbrs771085839
gwascentralrs771085839
openSNPrs771085839
23andMers771085839
23andMe allrs771085839
SNPshotrs771085839
SNPdbers771085839
MSV3drs771085839
GWAS Ctlgrs771085839
Max Magnitude0
ClinVar
Risk rs771085839(C;C)
Alt rs771085839(C;C)
Reference Rs771085839(G;G)
Significance Probable-Pathogenic
Disease Hereditary diffuse gastric cancer
Variation info
Gene CDH1
CLNDBN Hereditary diffuse gastric cancer
Reversed 0
HGVS NC_000016.9:g.68842595G>C
CLNSRC
CLNACC RCV000465136.1,