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rs587781384

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587781384(G;T)
Make rs587781384(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position94456323
GeneMRE11A
is asnp
is mentioned by
dbSNPrs587781384
ebirs587781384
HLIrs587781384
Exacrs587781384
Varsomers587781384
Maprs587781384
PheGenIrs587781384
hapmaprs587781384
1000 genomesrs587781384
hgdprs587781384
ensemblrs587781384
gopubmedrs587781384
geneviewrs587781384
scholarrs587781384
googlers587781384
pharmgkbrs587781384
gwascentralrs587781384
openSNPrs587781384
23andMers587781384
23andMe allrs587781384
SNP Nexus

SNPshotrs587781384
SNPdbers587781384
MSV3drs587781384
GWAS Ctlgrs587781384
Max Magnitude0
ClinVar
Risk rs587781384(A,T;A,T)
Alt rs587781384(A,T;A,T)
Reference rs587781384(G;G)
Significance Other
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MRE11A
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000011.9:g.94189489C>A; NC_000011.9:g.94189489C>T
CLNSRC
CLNACC RCV000129216.3, RCV000165707.1,