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rs137852762

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852762(A;A)
Make rs137852762(A;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position94459466
GeneMRE11A
is asnp
is mentioned by
dbSNPrs137852762
ebirs137852762
HLIrs137852762
Exacrs137852762
Varsomers137852762
Maprs137852762
PheGenIrs137852762
hapmaprs137852762
1000 genomesrs137852762
hgdprs137852762
ensemblrs137852762
gopubmedrs137852762
geneviewrs137852762
scholarrs137852762
googlers137852762
pharmgkbrs137852762
gwascentralrs137852762
openSNPrs137852762
23andMers137852762
23andMe allrs137852762
SNP Nexus

SNPshotrs137852762
SNPdbers137852762
MSV3drs137852762
GWAS Ctlgrs137852762
Max Magnitude0
OMIM600814
Desc
Variant0004
Relatedalso
ClinVar
Risk rs137852762(A;A)
Alt rs137852762(A;A)
Reference rs137852762(C;C)
Significance Pathogenic
Disease Ataxia-telangiectasia-like disorder
Variation info
Gene MRE11A
CLNDBN Ataxia-telangiectasia-like disorder
Reversed 1
HGVS NC_000011.9:g.94192632G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009330.2,