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rs587779815

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779815(C;T)
Make rs587779815(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108250804
GeneATM
is asnp
is mentioned by
dbSNPrs587779815
ebirs587779815
HLIrs587779815
Exacrs587779815
Varsomers587779815
Maprs587779815
PheGenIrs587779815
hapmaprs587779815
1000 genomesrs587779815
hgdprs587779815
ensemblrs587779815
gopubmedrs587779815
geneviewrs587779815
scholarrs587779815
googlers587779815
pharmgkbrs587779815
gwascentralrs587779815
openSNPrs587779815
23andMers587779815
23andMe allrs587779815
SNP Nexus

SNPshotrs587779815
SNPdbers587779815
MSV3drs587779815
GWAS Ctlgrs587779815
Max Magnitude0
ClinVar
Risk rs587779815(T;T)
Alt rs587779815(T;T)
Reference rs587779815(C;C)
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.108121531C>T
CLNSRC
CLNACC RCV000115141.5, RCV000169409.1, RCV000211960.2,