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rs876660289

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876660289(-;-)
Make rs876660289(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108301788
GeneATM
is asnp
is mentioned by
dbSNPrs876660289
ebirs876660289
HLIrs876660289
Exacrs876660289
Varsomers876660289
Maprs876660289
PheGenIrs876660289
hapmaprs876660289
1000 genomesrs876660289
hgdprs876660289
ensemblrs876660289
gopubmedrs876660289
geneviewrs876660289
scholarrs876660289
googlers876660289
pharmgkbrs876660289
gwascentralrs876660289
openSNPrs876660289
23andMers876660289
23andMe allrs876660289
SNP Nexus

SNPshotrs876660289
SNPdbers876660289
MSV3drs876660289
GWAS Ctlgrs876660289
Max Magnitude0
ClinVar
Risk rs876660289(;)
Alt rs876660289(;)
Reference rs876660289(A;A)
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.108172515delA
CLNSRC
CLNACC RCV000217025.1,