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rs370345996

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs370345996(A;A)
Make rs370345996(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position68829757
GeneCDH1
is asnp
is mentioned by
dbSNPrs370345996
ebirs370345996
HLIrs370345996
Exacrs370345996
Varsomers370345996
Maprs370345996
PheGenIrs370345996
hapmaprs370345996
1000 genomesrs370345996
hgdprs370345996
ensemblrs370345996
gopubmedrs370345996
geneviewrs370345996
scholarrs370345996
googlers370345996
pharmgkbrs370345996
gwascentralrs370345996
openSNPrs370345996
23andMers370345996
23andMe allrs370345996
SNP Nexus

SNPshotrs370345996
SNPdbers370345996
MSV3drs370345996
GWAS Ctlgrs370345996
Max Magnitude0
ClinVar
Risk rs370345996(A,C;A,C)
Alt rs370345996(A,C;A,C)
Reference rs370345996(G;G)
Significance Unknown
Disease Hereditary cancer-predisposing syndrome Hereditary diffuse gastric cancer not specified
Variation info
Gene CDH1
CLNDBN Hereditary cancer-predisposing syndrome Hereditary diffuse gastric cancer not specified
Reversed 0
HGVS NC_000016.9:g.68863660G>A
CLNSRC
CLNACC RCV000131445.4, RCV000198268.1, RCV000212387.1,