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rs730881296

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881296(-;-)
Make rs730881296(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108235706
GeneATM
is asnp
is mentioned by
dbSNPrs730881296
ebirs730881296
HLIrs730881296
Exacrs730881296
Varsomers730881296
Maprs730881296
PheGenIrs730881296
hapmaprs730881296
1000 genomesrs730881296
hgdprs730881296
ensemblrs730881296
gopubmedrs730881296
geneviewrs730881296
scholarrs730881296
googlers730881296
pharmgkbrs730881296
gwascentralrs730881296
openSNPrs730881296
23andMers730881296
23andMe allrs730881296
SNP Nexus

SNPshotrs730881296
SNPdbers730881296
MSV3drs730881296
GWAS Ctlgrs730881296
Max Magnitude0
ClinVar
Risk rs730881296(;)
Alt rs730881296(;)
Reference rs730881296(A;A)
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.108106433delA
CLNSRC
CLNACC RCV000159625.1, RCV000216666.1, RCV000233291.1,