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rs878853522

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853522(-;-)
Make rs878853522(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108302976
GeneATM
is asnp
is mentioned by
dbSNPrs878853522
ebirs878853522
HLIrs878853522
Exacrs878853522
Varsomers878853522
Maprs878853522
PheGenIrs878853522
hapmaprs878853522
1000 genomesrs878853522
hgdprs878853522
ensemblrs878853522
gopubmedrs878853522
geneviewrs878853522
scholarrs878853522
googlers878853522
pharmgkbrs878853522
gwascentralrs878853522
openSNPrs878853522
23andMers878853522
23andMe allrs878853522
SNP Nexus

SNPshotrs878853522
SNPdbers878853522
MSV3drs878853522
GWAS Ctlgrs878853522
Max Magnitude0
ClinVar
Risk rs878853522(;)
Alt rs878853522(;)
Reference rs878853522(G;G)
Significance Pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108173703delG
CLNSRC
CLNACC RCV000226250.1,