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rs587779852

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779852(G;T)
Make rs587779852(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108312424
GeneATM
is asnp
is mentioned by
dbSNPrs587779852
ebirs587779852
HLIrs587779852
Exacrs587779852
Varsomers587779852
Maprs587779852
PheGenIrs587779852
hapmaprs587779852
1000 genomesrs587779852
hgdprs587779852
ensemblrs587779852
gopubmedrs587779852
geneviewrs587779852
scholarrs587779852
googlers587779852
pharmgkbrs587779852
gwascentralrs587779852
openSNPrs587779852
23andMers587779852
23andMe allrs587779852
SNP Nexus

SNPshotrs587779852
SNPdbers587779852
MSV3drs587779852
GWAS Ctlgrs587779852
Max Magnitude0
ClinVar
Risk rs587779852(T;T)
Alt rs587779852(T;T)
Reference rs587779852(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108183151G>T
CLNSRC
CLNACC RCV000115219.5, RCV000205725.1, RCV000212035.1,