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rs587782558

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587782558(-;-)
Make rs587782558(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108345756
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs587782558
ebirs587782558
HLIrs587782558
Exacrs587782558
Varsomers587782558
Maprs587782558
PheGenIrs587782558
hapmaprs587782558
1000 genomesrs587782558
hgdprs587782558
ensemblrs587782558
gopubmedrs587782558
geneviewrs587782558
scholarrs587782558
googlers587782558
pharmgkbrs587782558
gwascentralrs587782558
openSNPrs587782558
23andMers587782558
23andMe allrs587782558
SNP Nexus

SNPshotrs587782558
SNPdbers587782558
MSV3drs587782558
GWAS Ctlgrs587782558
Max Magnitude0
ClinVar
Risk rs587782558(;)
Alt rs587782558(;)
Reference rs587782558(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108216483delA
CLNSRC
CLNACC RCV000131776.2, RCV000229908.1, RCV000235769.1,