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rs878854776

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878854776(A;G)
Make rs878854776(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position94459583
GeneMRE11
is asnp
is mentioned by
dbSNPrs878854776
ebirs878854776
HLIrs878854776
Exacrs878854776
Varsomers878854776
Maprs878854776
PheGenIrs878854776
hapmaprs878854776
1000 genomesrs878854776
hgdprs878854776
ensemblrs878854776
gopubmedrs878854776
geneviewrs878854776
scholarrs878854776
googlers878854776
pharmgkbrs878854776
gwascentralrs878854776
openSNPrs878854776
23andMers878854776
23andMe allrs878854776
SNP Nexus

SNPshotrs878854776
SNPdbers878854776
MSV3drs878854776
GWAS Ctlgrs878854776
Max Magnitude0
ClinVar
Risk rs878854776(G;G)
Alt rs878854776(G;G)
Reference rs878854776(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MRE11A
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000011.9:g.94192749T>C
CLNSRC
CLNACC RCV000226518.1,