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rs587781911

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587781911(G;T)
Make rs587781911(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108279594
GeneATM
is asnp
is mentioned by
dbSNPrs587781911
ebirs587781911
HLIrs587781911
Exacrs587781911
Varsomers587781911
Maprs587781911
PheGenIrs587781911
hapmaprs587781911
1000 genomesrs587781911
hgdprs587781911
ensemblrs587781911
gopubmedrs587781911
geneviewrs587781911
scholarrs587781911
googlers587781911
pharmgkbrs587781911
gwascentralrs587781911
openSNPrs587781911
23andMers587781911
23andMe allrs587781911
SNP Nexus

SNPshotrs587781911
SNPdbers587781911
MSV3drs587781911
GWAS Ctlgrs587781911
Max Magnitude0
ClinVar
Risk rs587781911(T;T)
Alt rs587781911(T;T)
Reference rs587781911(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.108150321G>T
CLNSRC
CLNACC RCV000130253.2,