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rs587782192

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587782192(G;G)
Make rs587782192(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108284460
GeneATM
is asnp
is mentioned by
dbSNPrs587782192
ebirs587782192
HLIrs587782192
Exacrs587782192
Varsomers587782192
Maprs587782192
PheGenIrs587782192
hapmaprs587782192
1000 genomesrs587782192
hgdprs587782192
ensemblrs587782192
gopubmedrs587782192
geneviewrs587782192
scholarrs587782192
googlers587782192
pharmgkbrs587782192
gwascentralrs587782192
openSNPrs587782192
23andMers587782192
23andMe allrs587782192
SNP Nexus

SNPshotrs587782192
SNPdbers587782192
MSV3drs587782192
GWAS Ctlgrs587782192
Max Magnitude0
ClinVar
Risk rs587782192(G;G)
Alt rs587782192(G;G)
Reference rs587782192(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108155187T>G
CLNSRC
CLNACC RCV000130840.2,