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rs876660933

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660933(G;T)
Make rs876660933(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108244954
GeneATM
is asnp
is mentioned by
dbSNPrs876660933
ebirs876660933
HLIrs876660933
Exacrs876660933
Varsomers876660933
Maprs876660933
PheGenIrs876660933
hapmaprs876660933
1000 genomesrs876660933
hgdprs876660933
ensemblrs876660933
gopubmedrs876660933
geneviewrs876660933
scholarrs876660933
googlers876660933
pharmgkbrs876660933
gwascentralrs876660933
openSNPrs876660933
23andMers876660933
23andMe allrs876660933
SNP Nexus

SNPshotrs876660933
SNPdbers876660933
MSV3drs876660933
GWAS Ctlgrs876660933
Max Magnitude0
ClinVar
Risk rs876660933(T;T)
Alt rs876660933(T;T)
Reference rs876660933(G;G)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations not provided
Variation info
Gene ATM
CLNDBN Tumor susceptibility linked to germline BAP1 mutations not provided
Reversed 0
HGVS NC_000011.9:g.108115681G>T
CLNSRC
CLNACC RCV000223320.1, RCV000235851.1,