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rs587782812

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782812(-;-)
Make rs587782812(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108302929
GeneATM
is asnp
is mentioned by
dbSNPrs587782812
ebirs587782812
HLIrs587782812
Exacrs587782812
Varsomers587782812
Maprs587782812
PheGenIrs587782812
hapmaprs587782812
1000 genomesrs587782812
hgdprs587782812
ensemblrs587782812
gopubmedrs587782812
geneviewrs587782812
scholarrs587782812
googlers587782812
pharmgkbrs587782812
gwascentralrs587782812
openSNPrs587782812
23andMers587782812
23andMe allrs587782812
SNP Nexus

SNPshotrs587782812
SNPdbers587782812
MSV3drs587782812
GWAS Ctlgrs587782812
Max Magnitude0
ClinVar
Risk rs587782812(;)
Alt rs587782812(;)
Reference rs587782812(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.108173656delG
CLNSRC
CLNACC RCV000132379.2,