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rs796051858

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796051858(A;A)
Make rs796051858(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108235839
GeneATM
is asnp
is mentioned by
dbSNPrs796051858
ebirs796051858
HLIrs796051858
Exacrs796051858
Varsomers796051858
Maprs796051858
PheGenIrs796051858
hapmaprs796051858
1000 genomesrs796051858
hgdprs796051858
ensemblrs796051858
gopubmedrs796051858
geneviewrs796051858
scholarrs796051858
googlers796051858
pharmgkbrs796051858
gwascentralrs796051858
openSNPrs796051858
23andMers796051858
23andMe allrs796051858
SNP Nexus

SNPshotrs796051858
SNPdbers796051858
MSV3drs796051858
GWAS Ctlgrs796051858
Max Magnitude0
ClinVar
Risk rs796051858(A;A)
Alt rs796051858(A;A)
Reference rs796051858(G;G)
Significance Pathogenic
Disease Ataxia-telangiectasia variant Tumor susceptibility linked to germline BAP1 mutations not provided
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia variant Tumor susceptibility linked to germline BAP1 mutations not provided
Reversed 0
HGVS NC_000011.9:g.108106566G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003188.3, RCV000213739.1, RCV000235952.1,