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rs587782844

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587782844(-;-)
Make rs587782844(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108250794
GeneATM
is asnp
is mentioned by
dbSNPrs587782844
ebirs587782844
HLIrs587782844
Exacrs587782844
Varsomers587782844
Maprs587782844
PheGenIrs587782844
hapmaprs587782844
1000 genomesrs587782844
hgdprs587782844
ensemblrs587782844
gopubmedrs587782844
geneviewrs587782844
scholarrs587782844
googlers587782844
pharmgkbrs587782844
gwascentralrs587782844
openSNPrs587782844
23andMers587782844
23andMe allrs587782844
SNP Nexus

SNPshotrs587782844
SNPdbers587782844
MSV3drs587782844
GWAS Ctlgrs587782844
Max Magnitude0
ClinVar
Risk rs587782844(;)
Alt rs587782844(;)
Reference rs587782844(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.108121521delA
CLNSRC
CLNACC RCV000132438.2,