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rs587782280

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782280(G;T)
Make rs587782280(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108267252
GeneATM
is asnp
is mentioned by
dbSNPrs587782280
ebirs587782280
HLIrs587782280
Exacrs587782280
Varsomers587782280
Maprs587782280
PheGenIrs587782280
hapmaprs587782280
1000 genomesrs587782280
hgdprs587782280
ensemblrs587782280
gopubmedrs587782280
geneviewrs587782280
scholarrs587782280
googlers587782280
pharmgkbrs587782280
gwascentralrs587782280
openSNPrs587782280
23andMers587782280
23andMe allrs587782280
SNP Nexus

SNPshotrs587782280
SNPdbers587782280
MSV3drs587782280
GWAS Ctlgrs587782280
Max Magnitude0
ClinVar
Risk rs587782280(T;T)
Alt rs587782280(T;T)
Reference rs587782280(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108137979G>T
CLNSRC
CLNACC RCV000131140.2,