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rs587781584

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587781584(A;A)
Make rs587781584(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108315912
GeneATM
is asnp
is mentioned by
dbSNPrs587781584
ebirs587781584
HLIrs587781584
Exacrs587781584
Varsomers587781584
Maprs587781584
PheGenIrs587781584
hapmaprs587781584
1000 genomesrs587781584
hgdprs587781584
ensemblrs587781584
gopubmedrs587781584
geneviewrs587781584
scholarrs587781584
googlers587781584
pharmgkbrs587781584
gwascentralrs587781584
openSNPrs587781584
23andMers587781584
23andMe allrs587781584
SNP Nexus

SNPshotrs587781584
SNPdbers587781584
MSV3drs587781584
GWAS Ctlgrs587781584
Max Magnitude0
ClinVar
Risk rs587781584(A;A)
Alt rs587781584(A;A)
Reference rs587781584(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108186639G>A
CLNSRC
CLNACC RCV000129624.2,