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rs587782103

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782103(A;A)
Make rs587782103(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108271406
GeneATM
is asnp
is mentioned by
dbSNPrs587782103
ebirs587782103
HLIrs587782103
Exacrs587782103
Varsomers587782103
Maprs587782103
PheGenIrs587782103
hapmaprs587782103
1000 genomesrs587782103
hgdprs587782103
ensemblrs587782103
gopubmedrs587782103
geneviewrs587782103
scholarrs587782103
googlers587782103
pharmgkbrs587782103
gwascentralrs587782103
openSNPrs587782103
23andMers587782103
23andMe allrs587782103
SNP Nexus

SNPshotrs587782103
SNPdbers587782103
MSV3drs587782103
GWAS Ctlgrs587782103
Max Magnitude0
ClinVar
Risk rs587782103(A;A)
Alt rs587782103(A;A)
Reference rs587782103(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108142133G>A
CLNSRC
CLNACC RCV000130616.2,