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rs587782308

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587782308(C;T)
Make rs587782308(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position94478782
GeneMRE11A
is asnp
is mentioned by
dbSNPrs587782308
ebirs587782308
HLIrs587782308
Exacrs587782308
Varsomers587782308
Maprs587782308
PheGenIrs587782308
hapmaprs587782308
1000 genomesrs587782308
hgdprs587782308
ensemblrs587782308
gopubmedrs587782308
geneviewrs587782308
scholarrs587782308
googlers587782308
pharmgkbrs587782308
gwascentralrs587782308
openSNPrs587782308
23andMers587782308
23andMe allrs587782308
SNP Nexus

SNPshotrs587782308
SNPdbers587782308
MSV3drs587782308
GWAS Ctlgrs587782308
Max Magnitude0
ClinVar
Risk rs587782308(T;T)
Alt rs587782308(T;T)
Reference rs587782308(C;C)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia-like disorder
Variation info
Gene MRE11A
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia-like disorder
Reversed 1
HGVS NC_000011.9:g.94211948G>A
CLNSRC
CLNACC RCV000131199.2, RCV000199534.1,