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rs137852761

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852761(C;T)
Make rs137852761(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position94447288
GeneMRE11A
is asnp
is mentioned by
dbSNPrs137852761
ebirs137852761
HLIrs137852761
Exacrs137852761
Varsomers137852761
Maprs137852761
PheGenIrs137852761
hapmaprs137852761
1000 genomesrs137852761
hgdprs137852761
ensemblrs137852761
gopubmedrs137852761
geneviewrs137852761
scholarrs137852761
googlers137852761
pharmgkbrs137852761
gwascentralrs137852761
openSNPrs137852761
23andMers137852761
23andMe allrs137852761
SNP Nexus

SNPshotrs137852761
SNPdbers137852761
MSV3drs137852761
GWAS Ctlgrs137852761
Max Magnitude0
OMIM600814
Desc
Variant0003
Relatedalso
ClinVar
Risk rs137852761(T;T)
Alt rs137852761(T;T)
Reference rs137852761(C;C)
Significance Pathogenic
Disease Ataxia-telangiectasia-like disorder Hereditary cancer-predisposing syndrome
Variation info
Gene MRE11A
CLNDBN Ataxia-telangiectasia-like disorder Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000011.9:g.94180454G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009329.3, RCV000130661.2,