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rs878853495

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878853495(A;A)
Make rs878853495(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108259077
GeneATM
is asnp
is mentioned by
dbSNPrs878853495
ebirs878853495
HLIrs878853495
Exacrs878853495
Varsomers878853495
Maprs878853495
PheGenIrs878853495
hapmaprs878853495
1000 genomesrs878853495
hgdprs878853495
ensemblrs878853495
gopubmedrs878853495
geneviewrs878853495
scholarrs878853495
googlers878853495
pharmgkbrs878853495
gwascentralrs878853495
openSNPrs878853495
23andMers878853495
23andMe allrs878853495
SNP Nexus

SNPshotrs878853495
SNPdbers878853495
MSV3drs878853495
GWAS Ctlgrs878853495
Max Magnitude0
ClinVar
Risk rs878853495(A;A)
Alt rs878853495(A;A)
Reference rs878853495(T;T)
Significance Probable-Pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108129804T>A
CLNSRC
CLNACC RCV000234163.1,