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rs869312754

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312754(G;T)
Make rs869312754(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108227594
GeneATM
is asnp
is mentioned by
dbSNPrs869312754
ebirs869312754
HLIrs869312754
Exacrs869312754
Varsomers869312754
Maprs869312754
PheGenIrs869312754
hapmaprs869312754
1000 genomesrs869312754
hgdprs869312754
ensemblrs869312754
gopubmedrs869312754
geneviewrs869312754
scholarrs869312754
googlers869312754
pharmgkbrs869312754
gwascentralrs869312754
openSNPrs869312754
23andMers869312754
23andMe allrs869312754
SNP Nexus

SNPshotrs869312754
SNPdbers869312754
MSV3drs869312754
GWAS Ctlgrs869312754
Max Magnitude0
ClinVar
Risk rs869312754(T;T)
Alt rs869312754(T;T)
Reference rs869312754(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108098321G>T
CLNSRC
CLNACC RCV000210108.1,