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rs587781752

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587781752(-;-)
Make rs587781752(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108279575
GeneATM
is asnp
is mentioned by
dbSNPrs587781752
ebirs587781752
HLIrs587781752
Exacrs587781752
Varsomers587781752
Maprs587781752
PheGenIrs587781752
hapmaprs587781752
1000 genomesrs587781752
hgdprs587781752
ensemblrs587781752
gopubmedrs587781752
geneviewrs587781752
scholarrs587781752
googlers587781752
pharmgkbrs587781752
gwascentralrs587781752
openSNPrs587781752
23andMers587781752
23andMe allrs587781752
SNP Nexus

SNPshotrs587781752
SNPdbers587781752
MSV3drs587781752
GWAS Ctlgrs587781752
Max Magnitude0
ClinVar
Risk rs587781752(;)
Alt rs587781752(;)
Reference rs587781752(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108150302delA
CLNSRC
CLNACC RCV000129958.2,