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rs786202151

From SNPedia

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


Make rs786202151(-;-)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position68801708
GeneCDH1
is asnp
is mentioned by
dbSNPrs786202151
ebirs786202151
HLIrs786202151
Exacrs786202151
Varsomers786202151
Maprs786202151
PheGenIrs786202151
hapmaprs786202151
1000 genomesrs786202151
hgdprs786202151
ensemblrs786202151
gopubmedrs786202151
geneviewrs786202151
scholarrs786202151
googlers786202151
pharmgkbrs786202151
gwascentralrs786202151
openSNPrs786202151
23andMers786202151
23andMe allrs786202151
SNP Nexus

SNPshotrs786202151
SNPdbers786202151
MSV3drs786202151
GWAS Ctlgrs786202151
Max Magnitude5
ClinVar
Risk rs786202151(;)
Alt rs786202151(;)
Reference rs786202151(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene CDH1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000016.9:g.68835611delT
CLNSRC
CLNACC RCV000164820.1,