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rs878854491

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878854491(C;T)
Make rs878854491(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47377045
GeneEPCAM, MIR559
is asnp
is mentioned by
dbSNPrs878854491
ebirs878854491
HLIrs878854491
Exacrs878854491
Varsomers878854491
Maprs878854491
PheGenIrs878854491
hapmaprs878854491
1000 genomesrs878854491
hgdprs878854491
ensemblrs878854491
gopubmedrs878854491
geneviewrs878854491
scholarrs878854491
googlers878854491
pharmgkbrs878854491
gwascentralrs878854491
openSNPrs878854491
23andMers878854491
23andMe allrs878854491
SNP Nexus

SNPshotrs878854491
SNPdbers878854491
MSV3drs878854491
GWAS Ctlgrs878854491
Max Magnitude0
ClinVar
Risk rs878854491(T;T)
Alt rs878854491(T;T)
Reference rs878854491(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene EPCAM MIR559
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47604184C>T
CLNSRC
CLNACC RCV000227834.1,