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rs587781299

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587781299(-;-)
Make rs587781299(-;A)
Make rs587781299(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108327666
GeneATM
is asnp
is mentioned by
dbSNPrs587781299
ebirs587781299
HLIrs587781299
Exacrs587781299
Varsomers587781299
Maprs587781299
PheGenIrs587781299
hapmaprs587781299
1000 genomesrs587781299
hgdprs587781299
ensemblrs587781299
gopubmedrs587781299
geneviewrs587781299
scholarrs587781299
googlers587781299
pharmgkbrs587781299
gwascentralrs587781299
openSNPrs587781299
23andMers587781299
23andMe allrs587781299
SNP Nexus

SNPshotrs587781299
SNPdbers587781299
MSV3drs587781299
GWAS Ctlgrs587781299
Max Magnitude0
ClinVar
Risk rs587781299(A;A)
Alt rs587781299(A;A)
Reference rs587781299(;)
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.108198393dupA
CLNSRC
CLNACC RCV000129007.3, RCV000205392.2, RCV000236518.1,