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rs878853535

From SNPedia

Orientationplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs878853535(-;-)
Make rs878853535(-;AG)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108326166
GeneATM
is asnp
is mentioned by
dbSNPrs878853535
ebirs878853535
HLIrs878853535
Exacrs878853535
Varsomers878853535
Maprs878853535
PheGenIrs878853535
hapmaprs878853535
1000 genomesrs878853535
hgdprs878853535
ensemblrs878853535
gopubmedrs878853535
geneviewrs878853535
scholarrs878853535
googlers878853535
pharmgkbrs878853535
gwascentralrs878853535
openSNPrs878853535
23andMers878853535
23andMe allrs878853535
SNP Nexus

SNPshotrs878853535
SNPdbers878853535
MSV3drs878853535
GWAS Ctlgrs878853535
Max Magnitude0
ClinVar
Risk rs878853535(;)
Alt rs878853535(;)
Reference rs878853535(AG;AG)
Significance Pathogenic
Disease Ataxia-telangiectasia syndrome not provided
Variation info
Gene C11orf65 ATM
CLNDBN Ataxia-telangiectasia syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108196893_108196894delAG
CLNSRC
CLNACC RCV000234351.1, RCV000235684.1,