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rs587782276

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587782276(A;G)
Make rs587782276(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108287598
GeneATM
is asnp
is mentioned by
dbSNPrs587782276
ebirs587782276
HLIrs587782276
Exacrs587782276
Varsomers587782276
Maprs587782276
PheGenIrs587782276
hapmaprs587782276
1000 genomesrs587782276
hgdprs587782276
ensemblrs587782276
gopubmedrs587782276
geneviewrs587782276
scholarrs587782276
googlers587782276
pharmgkbrs587782276
gwascentralrs587782276
openSNPrs587782276
23andMers587782276
23andMe allrs587782276
SNP Nexus

SNPshotrs587782276
SNPdbers587782276
MSV3drs587782276
GWAS Ctlgrs587782276
Max Magnitude0
ClinVar
Risk rs587782276(G;G)
Alt rs587782276(G;G)
Reference rs587782276(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108158325A>G
CLNSRC
CLNACC RCV000131133.2, RCV000198837.2,