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rs869312756

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312756(G;T)
Make rs869312756(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108307985
GeneATM
is asnp
is mentioned by
dbSNPrs869312756
ebirs869312756
HLIrs869312756
Exacrs869312756
Varsomers869312756
Maprs869312756
PheGenIrs869312756
hapmaprs869312756
1000 genomesrs869312756
hgdprs869312756
ensemblrs869312756
gopubmedrs869312756
geneviewrs869312756
scholarrs869312756
googlers869312756
pharmgkbrs869312756
gwascentralrs869312756
openSNPrs869312756
23andMers869312756
23andMe allrs869312756
SNP Nexus

SNPshotrs869312756
SNPdbers869312756
MSV3drs869312756
GWAS Ctlgrs869312756
Max Magnitude0
ClinVar
Risk rs869312756(T;T)
Alt rs869312756(T;T)
Reference rs869312756(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations Ataxia-telangiectasia syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108178712G>T
CLNSRC
CLNACC RCV000210115.1, RCV000223416.1, RCV000229503.1,