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rs587781815

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587781815(A;A)
Make rs587781815(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108272852
GeneATM
is asnp
is mentioned by
dbSNPrs587781815
ebirs587781815
HLIrs587781815
Exacrs587781815
Varsomers587781815
Maprs587781815
PheGenIrs587781815
hapmaprs587781815
1000 genomesrs587781815
hgdprs587781815
ensemblrs587781815
gopubmedrs587781815
geneviewrs587781815
scholarrs587781815
googlers587781815
pharmgkbrs587781815
gwascentralrs587781815
openSNPrs587781815
23andMers587781815
23andMe allrs587781815
SNP Nexus

SNPshotrs587781815
SNPdbers587781815
MSV3drs587781815
GWAS Ctlgrs587781815
Max Magnitude0
ClinVar
Risk rs587781815(A;A)
Alt rs587781815(A;A)
Reference rs587781815(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108143579G>A
CLNSRC
CLNACC RCV000130088.2,