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rs587781927

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587781927(C;C)
Make rs587781927(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108293479
GeneATM
is asnp
is mentioned by
dbSNPrs587781927
ClinGenrs587781927
ebirs587781927
HLIrs587781927
Exacrs587781927
Varsomers587781927
Maprs587781927
PheGenIrs587781927
hapmaprs587781927
1000 genomesrs587781927
hgdprs587781927
ensemblrs587781927
gopubmedrs587781927
geneviewrs587781927
scholarrs587781927
googlers587781927
pharmgkbrs587781927
gwascentralrs587781927
openSNPrs587781927
23andMers587781927
23andMe allrs587781927
SNP Nexus

SNPshotrs587781927
SNPdbers587781927
MSV3drs587781927
GWAS Ctlgrs587781927
Max Magnitude0
ClinVar
Risk rs587781927(C;C)
Alt rs587781927(C;C)
Reference Rs587781927(T;T)
Significance Pathogenic
Disease Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome not provided
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108164206T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000003170.5, RCV000130284.3, RCV000235350.1,