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rs587781658

From SNPedia

Orientationplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs587781658(-;-)
Make rs587781658(-;CT)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108257514
GeneATM
is asnp
is mentioned by
dbSNPrs587781658
ebirs587781658
HLIrs587781658
Exacrs587781658
Varsomers587781658
Maprs587781658
PheGenIrs587781658
hapmaprs587781658
1000 genomesrs587781658
hgdprs587781658
ensemblrs587781658
gopubmedrs587781658
geneviewrs587781658
scholarrs587781658
googlers587781658
pharmgkbrs587781658
gwascentralrs587781658
openSNPrs587781658
23andMers587781658
23andMe allrs587781658
SNP Nexus

SNPshotrs587781658
SNPdbers587781658
MSV3drs587781658
GWAS Ctlgrs587781658
Max Magnitude0
ClinVar
Risk rs587781658(;)
Alt rs587781658(;)
Reference rs587781658(CT;CT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108128241_108128242delCT
CLNSRC
CLNACC RCV000129801.2, RCV000233154.1,