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rs876658740

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658740(A;A)
Make rs876658740(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108310195
GeneATM
is asnp
is mentioned by
dbSNPrs876658740
ClinGenrs876658740
ebirs876658740
HLIrs876658740
Exacrs876658740
Varsomers876658740
Maprs876658740
PheGenIrs876658740
hapmaprs876658740
1000 genomesrs876658740
hgdprs876658740
ensemblrs876658740
gopubmedrs876658740
geneviewrs876658740
scholarrs876658740
googlers876658740
pharmgkbrs876658740
gwascentralrs876658740
openSNPrs876658740
23andMers876658740
23andMe allrs876658740
SNP Nexus

SNPshotrs876658740
SNPdbers876658740
MSV3drs876658740
GWAS Ctlgrs876658740
Max Magnitude0
ClinVar
Risk rs876658740(A;A)
Alt rs876658740(A;A)
Reference Rs876658740(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108180922G>A
CLNSRC
CLNACC RCV000218884.1, RCV000409971.1,