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rs786202817

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786202817(C;C)
Make rs786202817(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position68812265
GeneCDH1
is asnp
is mentioned by
dbSNPrs786202817
ebirs786202817
HLIrs786202817
Exacrs786202817
Varsomers786202817
Maprs786202817
PheGenIrs786202817
hapmaprs786202817
1000 genomesrs786202817
hgdprs786202817
ensemblrs786202817
gopubmedrs786202817
geneviewrs786202817
scholarrs786202817
googlers786202817
pharmgkbrs786202817
gwascentralrs786202817
openSNPrs786202817
23andMers786202817
23andMe allrs786202817
SNP Nexus

SNPshotrs786202817
SNPdbers786202817
MSV3drs786202817
GWAS Ctlgrs786202817
Max Magnitude0
ClinVar
Risk rs786202817(C;C)
Alt rs786202817(C;C)
Reference rs786202817(T;T)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene CDH1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000016.9:g.68846168T>C
CLNSRC
CLNACC RCV000165833.1,