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rs587781822

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587781822(A;G)
Make rs587781822(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position94435901
GeneMRE11A
is asnp
is mentioned by
dbSNPrs587781822
ebirs587781822
HLIrs587781822
Exacrs587781822
Varsomers587781822
Maprs587781822
PheGenIrs587781822
hapmaprs587781822
1000 genomesrs587781822
hgdprs587781822
ensemblrs587781822
gopubmedrs587781822
geneviewrs587781822
scholarrs587781822
googlers587781822
pharmgkbrs587781822
gwascentralrs587781822
openSNPrs587781822
23andMers587781822
23andMe allrs587781822
SNP Nexus

SNPshotrs587781822
SNPdbers587781822
MSV3drs587781822
GWAS Ctlgrs587781822
Max Magnitude0
ClinVar
Risk rs587781822(G;G)
Alt rs587781822(G;G)
Reference rs587781822(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.94169067T>C
CLNSRC
CLNACC RCV000130102.3,