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rs587782124

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587782124(G;G)
Make rs587782124(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108252914
GeneATM
is asnp
is mentioned by
dbSNPrs587782124
ebirs587782124
HLIrs587782124
Exacrs587782124
Varsomers587782124
Maprs587782124
PheGenIrs587782124
hapmaprs587782124
1000 genomesrs587782124
hgdprs587782124
ensemblrs587782124
gopubmedrs587782124
geneviewrs587782124
scholarrs587782124
googlers587782124
pharmgkbrs587782124
gwascentralrs587782124
openSNPrs587782124
23andMers587782124
23andMe allrs587782124
SNP Nexus

SNPshotrs587782124
SNPdbers587782124
MSV3drs587782124
GWAS Ctlgrs587782124
Max Magnitude0
ClinVar
Risk rs587782124(G;G)
Alt rs587782124(G;G)
Reference rs587782124(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108123641T>G
CLNSRC
CLNACC RCV000130662.2, RCV000235311.1,