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rs587782085

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782085(-;-)
Make rs587782085(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108249025
GeneATM
is asnp
is mentioned by
dbSNPrs587782085
ebirs587782085
HLIrs587782085
Exacrs587782085
Varsomers587782085
Maprs587782085
PheGenIrs587782085
hapmaprs587782085
1000 genomesrs587782085
hgdprs587782085
ensemblrs587782085
gopubmedrs587782085
geneviewrs587782085
scholarrs587782085
googlers587782085
pharmgkbrs587782085
gwascentralrs587782085
openSNPrs587782085
23andMers587782085
23andMe allrs587782085
SNP Nexus

SNPshotrs587782085
SNPdbers587782085
MSV3drs587782085
GWAS Ctlgrs587782085
Max Magnitude0
ClinVar
Risk rs587782085(;)
Alt rs587782085(;)
Reference rs587782085(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.108119752delG
CLNSRC
CLNACC RCV000130585.2,