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rs587781545

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587781545(C;T)
Make rs587781545(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108229275
GeneATM
is asnp
is mentioned by
dbSNPrs587781545
ebirs587781545
HLIrs587781545
Exacrs587781545
Varsomers587781545
Maprs587781545
PheGenIrs587781545
hapmaprs587781545
1000 genomesrs587781545
hgdprs587781545
ensemblrs587781545
gopubmedrs587781545
geneviewrs587781545
scholarrs587781545
googlers587781545
pharmgkbrs587781545
gwascentralrs587781545
openSNPrs587781545
23andMers587781545
23andMe allrs587781545
SNP Nexus

SNPshotrs587781545
SNPdbers587781545
MSV3drs587781545
GWAS Ctlgrs587781545
Max Magnitude0
ClinVar
Risk rs587781545(A,T;A,T)
Alt rs587781545(A,T;A,T)
Reference rs587781545(C;C)
Significance Pathogenic
Disease not specified Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN not specified Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108100002C>A; NC_000011.9:g.108100002C>T
CLNSRC
CLNACC RCV000159724.3, RCV000229615.1, RCV000129559.2,