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rs587781950

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587781950(A;T)
Make rs587781950(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108289065
GeneATM
is asnp
is mentioned by
dbSNPrs587781950
ebirs587781950
HLIrs587781950
Exacrs587781950
Varsomers587781950
Maprs587781950
PheGenIrs587781950
hapmaprs587781950
1000 genomesrs587781950
hgdprs587781950
ensemblrs587781950
gopubmedrs587781950
geneviewrs587781950
scholarrs587781950
googlers587781950
pharmgkbrs587781950
gwascentralrs587781950
openSNPrs587781950
23andMers587781950
23andMe allrs587781950
SNP Nexus

SNPshotrs587781950
SNPdbers587781950
MSV3drs587781950
GWAS Ctlgrs587781950
Max Magnitude0
ClinVar
Risk rs587781950(T;T)
Alt rs587781950(T;T)
Reference rs587781950(A;A)
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.108159792A>T
CLNSRC
CLNACC RCV000130320.2, RCV000204266.1,