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rs587780119

From SNPedia

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Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587780119(A;T)
Make rs587780119(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position68829701
GeneCDH1
is asnp
is mentioned by
dbSNPrs587780119
ebirs587780119
HLIrs587780119
Exacrs587780119
Varsomers587780119
Maprs587780119
PheGenIrs587780119
hapmaprs587780119
1000 genomesrs587780119
hgdprs587780119
ensemblrs587780119
gopubmedrs587780119
geneviewrs587780119
scholarrs587780119
googlers587780119
pharmgkbrs587780119
gwascentralrs587780119
openSNPrs587780119
23andMers587780119
23andMe allrs587780119
SNP Nexus

SNPshotrs587780119
SNPdbers587780119
MSV3drs587780119
GWAS Ctlgrs587780119
Max Magnitude0
ClinVar
Risk rs587780119(G,T;G,T)
Alt rs587780119(G,T;G,T)
Reference rs587780119(A;A)
Significance Probable-non-pathogenic
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.68863604A>G; NC_000016.9:g.68863604A>T
CLNSRC
CLNACC RCV000163882.1, RCV000115852.6, RCV000225693.1, RCV000234640.1,