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rs746703615

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs746703615(C;T)
Make rs746703615(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position68801883
GeneCDH1
is asnp
is mentioned by
dbSNPrs746703615
ebirs746703615
HLIrs746703615
Exacrs746703615
Varsomers746703615
Maprs746703615
PheGenIrs746703615
hapmaprs746703615
1000 genomesrs746703615
hgdprs746703615
ensemblrs746703615
gopubmedrs746703615
geneviewrs746703615
scholarrs746703615
googlers746703615
pharmgkbrs746703615
gwascentralrs746703615
openSNPrs746703615
23andMers746703615
23andMe allrs746703615
SNP Nexus

SNPshotrs746703615
SNPdbers746703615
MSV3drs746703615
GWAS Ctlgrs746703615
Max Magnitude0
ClinVar
Risk rs746703615(A,G,T;A,G,T)
Alt rs746703615(A,G,T;A,G,T)
Reference rs746703615(C;C)
Significance Unknown
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene CDH1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000016.9:g.68835786C>T
CLNSRC
CLNACC RCV000163916.1,