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rs587781381

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587781381(A;A)
Make rs587781381(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position94471572
GeneMRE11A
is asnp
is mentioned by
dbSNPrs587781381
ebirs587781381
HLIrs587781381
Exacrs587781381
Varsomers587781381
Maprs587781381
PheGenIrs587781381
hapmaprs587781381
1000 genomesrs587781381
hgdprs587781381
ensemblrs587781381
gopubmedrs587781381
geneviewrs587781381
scholarrs587781381
googlers587781381
pharmgkbrs587781381
gwascentralrs587781381
openSNPrs587781381
23andMers587781381
23andMe allrs587781381
SNP Nexus

SNPshotrs587781381
SNPdbers587781381
MSV3drs587781381
GWAS Ctlgrs587781381
Max Magnitude0
ClinVar
Risk rs587781381(A;A)
Alt rs587781381(A;A)
Reference rs587781381(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MRE11A
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000011.9:g.94204738A>T
CLNSRC
CLNACC RCV000129209.2,