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rs587781672

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587781672(G;T)
Make rs587781672(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108329027
GeneATM
is asnp
is mentioned by
dbSNPrs587781672
ebirs587781672
HLIrs587781672
Exacrs587781672
Varsomers587781672
Maprs587781672
PheGenIrs587781672
hapmaprs587781672
1000 genomesrs587781672
hgdprs587781672
ensemblrs587781672
gopubmedrs587781672
geneviewrs587781672
scholarrs587781672
googlers587781672
pharmgkbrs587781672
gwascentralrs587781672
openSNPrs587781672
23andMers587781672
23andMe allrs587781672
SNP Nexus

SNPshotrs587781672
SNPdbers587781672
MSV3drs587781672
GWAS Ctlgrs587781672
Max Magnitude0
ClinVar
Risk rs587781672(T;T)
Alt rs587781672(T;T)
Reference rs587781672(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108199754G>T
CLNSRC
CLNACC RCV000129830.2, RCV000169152.1,