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rs876660842

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876660842(-;-)
Make rs876660842(-;T)
Make rs876660842(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108227639
GeneATM
is asnp
is mentioned by
dbSNPrs876660842
ebirs876660842
HLIrs876660842
Exacrs876660842
Varsomers876660842
Maprs876660842
PheGenIrs876660842
hapmaprs876660842
1000 genomesrs876660842
hgdprs876660842
ensemblrs876660842
gopubmedrs876660842
geneviewrs876660842
scholarrs876660842
googlers876660842
pharmgkbrs876660842
gwascentralrs876660842
openSNPrs876660842
23andMers876660842
23andMe allrs876660842
SNP Nexus

SNPshotrs876660842
SNPdbers876660842
MSV3drs876660842
GWAS Ctlgrs876660842
Max Magnitude0
ClinVar
Risk rs876660842(T;T)
Alt rs876660842(T;T)
Reference rs876660842(;)
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.108098366dupT
CLNSRC
CLNACC RCV000213282.1,