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rs587781872

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587781872(-;-)
Make rs587781872(-;G)
Make rs587781872(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108325410
GeneATM
is asnp
is mentioned by
dbSNPrs587781872
ebirs587781872
HLIrs587781872
Exacrs587781872
Varsomers587781872
Maprs587781872
PheGenIrs587781872
hapmaprs587781872
1000 genomesrs587781872
hgdprs587781872
ensemblrs587781872
gopubmedrs587781872
geneviewrs587781872
scholarrs587781872
googlers587781872
pharmgkbrs587781872
gwascentralrs587781872
openSNPrs587781872
23andMers587781872
23andMe allrs587781872
SNP Nexus

SNPshotrs587781872
SNPdbers587781872
MSV3drs587781872
GWAS Ctlgrs587781872
Max Magnitude0
ClinVar
Risk rs587781872(G;G)
Alt rs587781872(G;G)
Reference rs587781872(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108196137dupG
CLNSRC
CLNACC RCV000130195.2,