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rs587781805

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587781805(-;-)
Make rs587781805(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108271107
GeneATM
is asnp
is mentioned by
dbSNPrs587781805
ebirs587781805
HLIrs587781805
Exacrs587781805
Varsomers587781805
Maprs587781805
PheGenIrs587781805
hapmaprs587781805
1000 genomesrs587781805
hgdprs587781805
ensemblrs587781805
gopubmedrs587781805
geneviewrs587781805
scholarrs587781805
googlers587781805
pharmgkbrs587781805
gwascentralrs587781805
openSNPrs587781805
23andMers587781805
23andMe allrs587781805
SNP Nexus

SNPshotrs587781805
SNPdbers587781805
MSV3drs587781805
GWAS Ctlgrs587781805
Max Magnitude0
ClinVar
Risk rs587781805(;)
Alt rs587781805(;)
Reference rs587781805(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.108141834delT
CLNSRC
CLNACC RCV000130076.2,