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rs869312755

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312755(C;T)
Make rs869312755(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108293436
GeneATM
is asnp
is mentioned by
dbSNPrs869312755
ebirs869312755
HLIrs869312755
Exacrs869312755
Varsomers869312755
Maprs869312755
PheGenIrs869312755
hapmaprs869312755
1000 genomesrs869312755
hgdprs869312755
ensemblrs869312755
gopubmedrs869312755
geneviewrs869312755
scholarrs869312755
googlers869312755
pharmgkbrs869312755
gwascentralrs869312755
openSNPrs869312755
23andMers869312755
23andMe allrs869312755
SNP Nexus

SNPshotrs869312755
SNPdbers869312755
MSV3drs869312755
GWAS Ctlgrs869312755
Max Magnitude0
ClinVar
Risk rs869312755(T;T)
Alt rs869312755(T;T)
Reference rs869312755(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108164163C>T
CLNSRC
CLNACC RCV000210197.1, RCV000222666.1, RCV000234068.1,