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rs730881667

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881667(C;T)
Make rs730881667(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position68819324
GeneCDH1
is asnp
is mentioned by
dbSNPrs730881667
ebirs730881667
HLIrs730881667
Exacrs730881667
Varsomers730881667
Maprs730881667
PheGenIrs730881667
hapmaprs730881667
1000 genomesrs730881667
hgdprs730881667
ensemblrs730881667
gopubmedrs730881667
geneviewrs730881667
scholarrs730881667
googlers730881667
pharmgkbrs730881667
gwascentralrs730881667
openSNPrs730881667
23andMers730881667
23andMe allrs730881667
SNP Nexus

SNPshotrs730881667
SNPdbers730881667
MSV3drs730881667
GWAS Ctlgrs730881667
Max Magnitude0
ClinVar
Risk rs730881667(T;T)
Alt rs730881667(T;T)
Reference rs730881667(C;C)
Significance Unknown
Disease Hereditary cancer-predisposing syndrome not specified Hereditary diffuse gastric cancer
Variation info
Gene CDH1
CLNDBN Hereditary cancer-predisposing syndrome not specified Hereditary diffuse gastric cancer
Reversed 0
HGVS NC_000016.9:g.68853227C>T
CLNSRC
CLNACC RCV000160393.3, RCV000212373.1, RCV000234355.1,