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rs587781984

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587781984(-;-)
Make rs587781984(-;T)
Make rs587781984(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108247115
GeneATM
is asnp
is mentioned by
dbSNPrs587781984
ebirs587781984
HLIrs587781984
Exacrs587781984
Varsomers587781984
Maprs587781984
PheGenIrs587781984
hapmaprs587781984
1000 genomesrs587781984
hgdprs587781984
ensemblrs587781984
gopubmedrs587781984
geneviewrs587781984
scholarrs587781984
googlers587781984
pharmgkbrs587781984
gwascentralrs587781984
openSNPrs587781984
23andMers587781984
23andMe allrs587781984
SNP Nexus

SNPshotrs587781984
SNPdbers587781984
MSV3drs587781984
GWAS Ctlgrs587781984
Max Magnitude0
ClinVar
Risk rs587781984(T;T)
Alt rs587781984(T;T)
Reference rs587781984(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108117842dupT
CLNSRC
CLNACC RCV000130384.2,