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rs587781978

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587781978(-;-)
Make rs587781978(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108244915
GeneATM
is asnp
is mentioned by
dbSNPrs587781978
ebirs587781978
HLIrs587781978
Exacrs587781978
Varsomers587781978
Maprs587781978
PheGenIrs587781978
hapmaprs587781978
1000 genomesrs587781978
hgdprs587781978
ensemblrs587781978
gopubmedrs587781978
geneviewrs587781978
scholarrs587781978
googlers587781978
pharmgkbrs587781978
gwascentralrs587781978
openSNPrs587781978
23andMers587781978
23andMe allrs587781978
SNP Nexus

SNPshotrs587781978
SNPdbers587781978
MSV3drs587781978
GWAS Ctlgrs587781978
Max Magnitude0
ClinVar
Risk rs587781978(;)
Alt rs587781978(;)
Reference rs587781978(T;T)
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.108115642delT
CLNSRC
CLNACC RCV000130373.2, RCV000233840.1, RCV000235917.1,