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rs587782114

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782114(A;A)
Make rs587782114(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108317500
GeneATM
is asnp
is mentioned by
dbSNPrs587782114
ebirs587782114
HLIrs587782114
Exacrs587782114
Varsomers587782114
Maprs587782114
PheGenIrs587782114
hapmaprs587782114
1000 genomesrs587782114
hgdprs587782114
ensemblrs587782114
gopubmedrs587782114
geneviewrs587782114
scholarrs587782114
googlers587782114
pharmgkbrs587782114
gwascentralrs587782114
openSNPrs587782114
23andMers587782114
23andMe allrs587782114
SNP Nexus

SNPshotrs587782114
SNPdbers587782114
MSV3drs587782114
GWAS Ctlgrs587782114
Max Magnitude0
ClinVar
Risk rs587782114(A;A)
Alt rs587782114(A;A)
Reference rs587782114(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108188227G>A
CLNSRC
CLNACC RCV000130633.2,