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rs876660741

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876660741(-;-)
Make rs876660741(-;T)
Make rs876660741(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108272786
GeneATM
is asnp
is mentioned by
dbSNPrs876660741
ebirs876660741
HLIrs876660741
Exacrs876660741
Varsomers876660741
Maprs876660741
PheGenIrs876660741
hapmaprs876660741
1000 genomesrs876660741
hgdprs876660741
ensemblrs876660741
gopubmedrs876660741
geneviewrs876660741
scholarrs876660741
googlers876660741
pharmgkbrs876660741
gwascentralrs876660741
openSNPrs876660741
23andMers876660741
23andMe allrs876660741
SNP Nexus

SNPshotrs876660741
SNPdbers876660741
MSV3drs876660741
GWAS Ctlgrs876660741
Max Magnitude0
ClinVar
Risk rs876660741(T;T)
Alt rs876660741(T;T)
Reference rs876660741(;)
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.108143513dupT
CLNSRC
CLNACC RCV000213678.1,