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rs876658583

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876658583(-;-)
Make rs876658583(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108257525
GeneATM
is asnp
is mentioned by
dbSNPrs876658583
dbSNP (old)rs876658583
ClinGenrs876658583
ebirs876658583
HLIrs876658583
Exacrs876658583
Gnomadrs876658583
Varsomers876658583
Maprs876658583
PheGenIrs876658583
Biobankrs876658583
1000 genomesrs876658583
hgdprs876658583
ensemblrs876658583
gopubmedrs876658583
geneviewrs876658583
scholarrs876658583
googlers876658583
pharmgkbrs876658583
gwascentralrs876658583
openSNPrs876658583
23andMers876658583
23andMe allrs876658583
SNP Nexus

SNPshotrs876658583
SNPdbers876658583
MSV3drs876658583
GWAS Ctlgrs876658583
Max Magnitude0
ClinVar
Risk rs876658583(-;-)
Alt rs876658583(-;-)
Reference Rs876658583(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108128252delT
CLNSRC
CLNACC RCV000222588.1,