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rs876659430

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876659430(C;C)
Make rs876659430(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108279610
GeneATM
is asnp
is mentioned by
dbSNPrs876659430
ebirs876659430
HLIrs876659430
Exacrs876659430
Varsomers876659430
Maprs876659430
PheGenIrs876659430
hapmaprs876659430
1000 genomesrs876659430
hgdprs876659430
ensemblrs876659430
gopubmedrs876659430
geneviewrs876659430
scholarrs876659430
googlers876659430
pharmgkbrs876659430
gwascentralrs876659430
openSNPrs876659430
23andMers876659430
23andMe allrs876659430
SNP Nexus

SNPshotrs876659430
SNPdbers876659430
MSV3drs876659430
GWAS Ctlgrs876659430
Max Magnitude0
ClinVar
Risk rs876659430(C;C)
Alt rs876659430(C;C)
Reference rs876659430(T;T)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene ATM
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000011.9:g.108150337T>C
CLNSRC
CLNACC RCV000215146.1,