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rs587781828

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587781828(-;-)
Make rs587781828(-;T)
Make rs587781828(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position94470564
GeneMRE11A
is asnp
is mentioned by
dbSNPrs587781828
ebirs587781828
HLIrs587781828
Exacrs587781828
Varsomers587781828
Maprs587781828
PheGenIrs587781828
hapmaprs587781828
1000 genomesrs587781828
hgdprs587781828
ensemblrs587781828
gopubmedrs587781828
geneviewrs587781828
scholarrs587781828
googlers587781828
pharmgkbrs587781828
gwascentralrs587781828
openSNPrs587781828
23andMers587781828
23andMe allrs587781828
SNP Nexus

SNPshotrs587781828
SNPdbers587781828
MSV3drs587781828
GWAS Ctlgrs587781828
Max Magnitude0
ClinVar
Risk rs587781828(T;T)
Alt rs587781828(T;T)
Reference rs587781828(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MRE11A
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000011.9:g.94203731dupA
CLNSRC
CLNACC RCV000130113.2,