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rs587781776

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587781776(-;-)
Make rs587781776(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108250820
GeneATM
is asnp
is mentioned by
dbSNPrs587781776
ebirs587781776
HLIrs587781776
Exacrs587781776
Varsomers587781776
Maprs587781776
PheGenIrs587781776
hapmaprs587781776
1000 genomesrs587781776
hgdprs587781776
ensemblrs587781776
gopubmedrs587781776
geneviewrs587781776
scholarrs587781776
googlers587781776
pharmgkbrs587781776
gwascentralrs587781776
openSNPrs587781776
23andMers587781776
23andMe allrs587781776
SNP Nexus

SNPshotrs587781776
SNPdbers587781776
MSV3drs587781776
GWAS Ctlgrs587781776
Max Magnitude0
ClinVar
Risk rs587781776(;)
Alt rs587781776(;)
Reference rs587781776(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108121547delC
CLNSRC
CLNACC RCV000130017.2,