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rs876659067

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876659067(C;T)
Make rs876659067(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108281103
GeneATM
is asnp
is mentioned by
dbSNPrs876659067
ebirs876659067
HLIrs876659067
Exacrs876659067
Varsomers876659067
Maprs876659067
PheGenIrs876659067
hapmaprs876659067
1000 genomesrs876659067
hgdprs876659067
ensemblrs876659067
gopubmedrs876659067
geneviewrs876659067
scholarrs876659067
googlers876659067
pharmgkbrs876659067
gwascentralrs876659067
openSNPrs876659067
23andMers876659067
23andMe allrs876659067
SNP Nexus

SNPshotrs876659067
SNPdbers876659067
MSV3drs876659067
GWAS Ctlgrs876659067
Max Magnitude0
ClinVar
Risk rs876659067(T;T)
Alt rs876659067(T;T)
Reference rs876659067(C;C)
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.108151830C>T
CLNSRC
CLNACC RCV000213580.1,