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rs751357509

From SNPedia

Merged intors587779817
Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs751357509(-;-)
Make rs751357509(-;AG)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108251026
GeneATM
is asnp
is mentioned by
dbSNPrs751357509
dbSNP (old)rs751357509
ClinGenrs751357509
ebirs751357509
HLIrs751357509
Exacrs751357509
Gnomadrs751357509
Varsomers751357509
Maprs751357509
PheGenIrs751357509
Biobankrs751357509
1000 genomesrs751357509
hgdprs751357509
ensemblrs751357509
gopubmedrs751357509
geneviewrs751357509
scholarrs751357509
googlers751357509
pharmgkbrs751357509
gwascentralrs751357509
openSNPrs751357509
23andMers751357509
23andMe allrs751357509
SNP Nexus

SNPshotrs751357509
SNPdbers751357509
MSV3drs751357509
GWAS Ctlgrs751357509
StatusMerged into rs587779817
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs751357509(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 RCV000115144.6, RCV000169147.3, RCV000211964.3,