Have questions? Visit https://www.reddit.com/r/SNPedia

rs587779833

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779833(C;G)
Make rs587779833(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108279578
GeneATM
is asnp
is mentioned by
dbSNPrs587779833
ebirs587779833
HLIrs587779833
Exacrs587779833
Varsomers587779833
Maprs587779833
PheGenIrs587779833
hapmaprs587779833
1000 genomesrs587779833
hgdprs587779833
ensemblrs587779833
gopubmedrs587779833
geneviewrs587779833
scholarrs587779833
googlers587779833
pharmgkbrs587779833
gwascentralrs587779833
openSNPrs587779833
23andMers587779833
23andMe allrs587779833
SNP Nexus

SNPshotrs587779833
SNPdbers587779833
MSV3drs587779833
GWAS Ctlgrs587779833
Max Magnitude0
ClinVar
Risk rs587779833(G;G)
Alt rs587779833(G;G)
Reference rs587779833(C;C)
Significance Other
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108150305C>G
CLNSRC
CLNACC RCV000115176.5, RCV000169463.2, RCV000211999.1,