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rs876660031

From SNPedia

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Geno Mag Summary
(;) 0 common in clinvar
Make rs876660031(-;-)
Make rs876660031(-;C)
Make rs876660031(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108279541
GeneATM
is asnp
is mentioned by
dbSNPrs876660031
ebirs876660031
HLIrs876660031
Exacrs876660031
Varsomers876660031
Maprs876660031
PheGenIrs876660031
hapmaprs876660031
1000 genomesrs876660031
hgdprs876660031
ensemblrs876660031
gopubmedrs876660031
geneviewrs876660031
scholarrs876660031
googlers876660031
pharmgkbrs876660031
gwascentralrs876660031
openSNPrs876660031
23andMers876660031
23andMe allrs876660031
SNP Nexus

SNPshotrs876660031
SNPdbers876660031
MSV3drs876660031
GWAS Ctlgrs876660031
Max Magnitude0
ClinVar
Risk rs876660031(C;C)
Alt rs876660031(C;C)
Reference rs876660031(;)
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.108150268dupC
CLNSRC
CLNACC RCV000222368.1,