Have questions? Visit https://www.reddit.com/r/SNPedia

rs587781449

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587781449(-;-)
Make rs587781449(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108235716
GeneATM
is asnp
is mentioned by
dbSNPrs587781449
ebirs587781449
HLIrs587781449
Exacrs587781449
Varsomers587781449
Maprs587781449
PheGenIrs587781449
hapmaprs587781449
1000 genomesrs587781449
hgdprs587781449
ensemblrs587781449
gopubmedrs587781449
geneviewrs587781449
scholarrs587781449
googlers587781449
pharmgkbrs587781449
gwascentralrs587781449
openSNPrs587781449
23andMers587781449
23andMe allrs587781449
SNP Nexus

SNPshotrs587781449
SNPdbers587781449
MSV3drs587781449
GWAS Ctlgrs587781449
Max Magnitude0
ClinVar
Risk rs587781449(;)
Alt rs587781449(;)
Reference rs587781449(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.108106443delT
CLNSRC
CLNACC RCV000129372.2,