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rs587782861

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587782861(-;-)
Make rs587782861(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108282758
GeneATM
is asnp
is mentioned by
dbSNPrs587782861
ebirs587782861
HLIrs587782861
Exacrs587782861
Varsomers587782861
Maprs587782861
PheGenIrs587782861
hapmaprs587782861
1000 genomesrs587782861
hgdprs587782861
ensemblrs587782861
gopubmedrs587782861
geneviewrs587782861
scholarrs587782861
googlers587782861
pharmgkbrs587782861
gwascentralrs587782861
openSNPrs587782861
23andMers587782861
23andMe allrs587782861
SNP Nexus

SNPshotrs587782861
SNPdbers587782861
MSV3drs587782861
GWAS Ctlgrs587782861
Max Magnitude0
ClinVar
Risk rs587782861(;)
Alt rs587782861(;)
Reference rs587782861(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108153485delT
CLNSRC
CLNACC RCV000132480.2,