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rs587779817

From SNPedia

Orientationplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs587779817(-;-)
Make rs587779817(-;GA)
Make rs587779817(GA;GA)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108251029
GeneATM
is asnp
is mentioned by
dbSNPrs587779817
ebirs587779817
HLIrs587779817
Exacrs587779817
Varsomers587779817
Maprs587779817
PheGenIrs587779817
hapmaprs587779817
1000 genomesrs587779817
hgdprs587779817
ensemblrs587779817
gopubmedrs587779817
geneviewrs587779817
scholarrs587779817
googlers587779817
pharmgkbrs587779817
gwascentralrs587779817
openSNPrs587779817
23andMers587779817
23andMe allrs587779817
SNP Nexus

SNPshotrs587779817
SNPdbers587779817
MSV3drs587779817
GWAS Ctlgrs587779817
Max Magnitude0
ClinVar
Risk rs587779817(;)
Alt rs587779817(;)
Reference rs587779817(AG;AG)
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.108121756_108121757delGA
CLNSRC
CLNACC RCV000115144.5, RCV000169147.3, RCV000211964.2,