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rs587781722

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587781722(C;T)
Make rs587781722(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108310305
GeneATM
is asnp
is mentioned by
dbSNPrs587781722
ebirs587781722
HLIrs587781722
Exacrs587781722
Varsomers587781722
Maprs587781722
PheGenIrs587781722
hapmaprs587781722
1000 genomesrs587781722
hgdprs587781722
ensemblrs587781722
gopubmedrs587781722
geneviewrs587781722
scholarrs587781722
googlers587781722
pharmgkbrs587781722
gwascentralrs587781722
openSNPrs587781722
23andMers587781722
23andMe allrs587781722
SNP Nexus

SNPshotrs587781722
SNPdbers587781722
MSV3drs587781722
GWAS Ctlgrs587781722
Max Magnitude0
ClinVar
Risk rs587781722(T;T)
Alt rs587781722(T;T)
Reference rs587781722(C;C)
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.108181032C>T
CLNSRC
CLNACC RCV000129909.2, RCV000200350.1, RCV000235704.1,