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rs878853530

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853530(-;-)
Make rs878853530(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108319979
GeneATM
is asnp
is mentioned by
dbSNPrs878853530
ebirs878853530
HLIrs878853530
Exacrs878853530
Varsomers878853530
Maprs878853530
PheGenIrs878853530
hapmaprs878853530
1000 genomesrs878853530
hgdprs878853530
ensemblrs878853530
gopubmedrs878853530
geneviewrs878853530
scholarrs878853530
googlers878853530
pharmgkbrs878853530
gwascentralrs878853530
openSNPrs878853530
23andMers878853530
23andMe allrs878853530
SNP Nexus

SNPshotrs878853530
SNPdbers878853530
MSV3drs878853530
GWAS Ctlgrs878853530
Max Magnitude0
ClinVar
Risk rs878853530(;)
Alt rs878853530(;)
Reference rs878853530(C;C)
Significance Pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108190706delC
CLNSRC
CLNACC RCV000229552.1,