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rs373226793

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs373226793(C;C)
Make rs373226793(C;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position108289735
GeneATM
is asnp
is mentioned by
dbSNPrs373226793
ebirs373226793
HLIrs373226793
Exacrs373226793
Varsomers373226793
Maprs373226793
PheGenIrs373226793
hapmaprs373226793
1000 genomesrs373226793
hgdprs373226793
ensemblrs373226793
gopubmedrs373226793
geneviewrs373226793
scholarrs373226793
googlers373226793
pharmgkbrs373226793
gwascentralrs373226793
openSNPrs373226793
23andMers373226793
23andMe allrs373226793
SNP Nexus

SNPshotrs373226793
SNPdbers373226793
MSV3drs373226793
GWAS Ctlgrs373226793
Max Magnitude0
ClinVar
Risk rs373226793(C,G;C,G)
Alt rs373226793(C,G;C,G)
Reference rs373226793(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108160462T>G
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000131174.2,