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rs786202290

From SNPedia

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Geno Mag Summary
(A;G) 5 Hereditary cancer-predisposing syndrome; gastric cancer related?
(G;G) 0 common in clinvar


Make rs786202290(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position68819425
GeneCDH1
is asnp
is mentioned by
dbSNPrs786202290
ebirs786202290
HLIrs786202290
Exacrs786202290
Varsomers786202290
Maprs786202290
PheGenIrs786202290
hapmaprs786202290
1000 genomesrs786202290
hgdprs786202290
ensemblrs786202290
gopubmedrs786202290
geneviewrs786202290
scholarrs786202290
googlers786202290
pharmgkbrs786202290
gwascentralrs786202290
openSNPrs786202290
23andMers786202290
23andMe allrs786202290
SNP Nexus

SNPshotrs786202290
SNPdbers786202290
MSV3drs786202290
GWAS Ctlgrs786202290
Max Magnitude5
ClinVar
Risk rs786202290(A;A)
Alt rs786202290(A;A)
Reference rs786202290(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene CDH1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000016.9:g.68853328G>A
CLNSRC
CLNACC RCV000165027.1,