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rs587782572

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587782572(-;-)
Make rs587782572(-;TA)
Make rs587782572(TA;TA)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108250698
GeneATM
is asnp
is mentioned by
dbSNPrs587782572
ebirs587782572
HLIrs587782572
Exacrs587782572
Varsomers587782572
Maprs587782572
PheGenIrs587782572
hapmaprs587782572
1000 genomesrs587782572
hgdprs587782572
ensemblrs587782572
gopubmedrs587782572
geneviewrs587782572
scholarrs587782572
googlers587782572
pharmgkbrs587782572
gwascentralrs587782572
openSNPrs587782572
23andMers587782572
23andMe allrs587782572
SNP Nexus

SNPshotrs587782572
SNPdbers587782572
MSV3drs587782572
GWAS Ctlgrs587782572
Max Magnitude0
ClinVar
Risk rs587782572(TA,TC,TTA;TA,TC,TTA)
Alt rs587782572(TA,TC,TTA;TA,TC,TTA)
Reference rs587782572(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.108121425_108121426delTA
CLNSRC
CLNACC RCV000131796.2,