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rs587779856

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779856(A;A)
Make rs587779856(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108321421
GeneATM
is asnp
is mentioned by
dbSNPrs587779856
ebirs587779856
HLIrs587779856
Exacrs587779856
Varsomers587779856
Maprs587779856
PheGenIrs587779856
hapmaprs587779856
1000 genomesrs587779856
hgdprs587779856
ensemblrs587779856
gopubmedrs587779856
geneviewrs587779856
scholarrs587779856
googlers587779856
pharmgkbrs587779856
gwascentralrs587779856
openSNPrs587779856
23andMers587779856
23andMe allrs587779856
SNP Nexus

SNPshotrs587779856
SNPdbers587779856
MSV3drs587779856
GWAS Ctlgrs587779856
Max Magnitude0
Mentioned as a pathogenic/likely pathogenic mutation associated with cancer predisposition in [PMID 26681312OA-icon.png]
ClinVar
Risk rs587779856(A;A)
Alt rs587779856(A;A)
Reference rs587779856(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108192148G>A
CLNSRC
CLNACC RCV000115231.5, RCV000212046.1,