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rs759520465

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs759520465(C;C)
Make rs759520465(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108292618
GeneATM
is asnp
is mentioned by
dbSNPrs759520465
ebirs759520465
HLIrs759520465
Exacrs759520465
Varsomers759520465
Maprs759520465
PheGenIrs759520465
hapmaprs759520465
1000 genomesrs759520465
hgdprs759520465
ensemblrs759520465
gopubmedrs759520465
geneviewrs759520465
scholarrs759520465
googlers759520465
pharmgkbrs759520465
gwascentralrs759520465
openSNPrs759520465
23andMers759520465
23andMe allrs759520465
SNP Nexus

SNPshotrs759520465
SNPdbers759520465
MSV3drs759520465
GWAS Ctlgrs759520465
Max Magnitude0
ClinVar
Risk rs759520465(C;C)
Alt rs759520465(C;C)
Reference Rs759520465(G;G)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108163345G>A; NC_000011.9:g.108163345G>C
CLNSRC
CLNACC RCV000255051.1, RCV000216400.1,