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rs587782030

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587782030(C;T)
Make rs587782030(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position94478771
GeneMRE11A
is asnp
is mentioned by
dbSNPrs587782030
ebirs587782030
HLIrs587782030
Exacrs587782030
Varsomers587782030
Maprs587782030
PheGenIrs587782030
hapmaprs587782030
1000 genomesrs587782030
hgdprs587782030
ensemblrs587782030
gopubmedrs587782030
geneviewrs587782030
scholarrs587782030
googlers587782030
pharmgkbrs587782030
gwascentralrs587782030
openSNPrs587782030
23andMers587782030
23andMe allrs587782030
SNP Nexus

SNPshotrs587782030
SNPdbers587782030
MSV3drs587782030
GWAS Ctlgrs587782030
Max Magnitude0
ClinVar
Risk rs587782030(A,T;A,T)
Alt rs587782030(A,T;A,T)
Reference rs587782030(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MRE11A
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000011.9:g.94211937G>A
CLNSRC
CLNACC RCV000130478.2,