Have questions? Visit https://www.reddit.com/r/SNPedia

rs876659039

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876659039(-;-)
Make rs876659039(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108293365
GeneATM
is asnp
is mentioned by
dbSNPrs876659039
ebirs876659039
HLIrs876659039
Exacrs876659039
Varsomers876659039
Maprs876659039
PheGenIrs876659039
hapmaprs876659039
1000 genomesrs876659039
hgdprs876659039
ensemblrs876659039
gopubmedrs876659039
geneviewrs876659039
scholarrs876659039
googlers876659039
pharmgkbrs876659039
gwascentralrs876659039
openSNPrs876659039
23andMers876659039
23andMe allrs876659039
SNP Nexus

SNPshotrs876659039
SNPdbers876659039
MSV3drs876659039
GWAS Ctlgrs876659039
Max Magnitude0
ClinVar
Risk rs876659039(;)
Alt rs876659039(;)
Reference rs876659039(T;T)
Significance 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.108164092delT
CLNSRC
CLNACC RCV000214193.1,