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rs587779834

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779834(-;-)
Make rs587779834(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108284282
GeneATM
is asnp
is mentioned by
dbSNPrs587779834
ebirs587779834
HLIrs587779834
Exacrs587779834
Varsomers587779834
Maprs587779834
PheGenIrs587779834
hapmaprs587779834
1000 genomesrs587779834
hgdprs587779834
ensemblrs587779834
gopubmedrs587779834
geneviewrs587779834
scholarrs587779834
googlers587779834
pharmgkbrs587779834
gwascentralrs587779834
openSNPrs587779834
23andMers587779834
23andMe allrs587779834
SNP Nexus

SNPshotrs587779834
SNPdbers587779834
MSV3drs587779834
GWAS Ctlgrs587779834
Max Magnitude0
ClinVar
Risk rs587779834(;)
Alt rs587779834(;)
Reference rs587779834(G;G)
Significance Pathogenic
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.108155009delG
CLNSRC
CLNACC RCV000115179.5, RCV000198788.3, RCV000212002.1,