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rs876658415

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876658415(A;G)
Make rs876658415(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108315872
GeneATM
is asnp
is mentioned by
dbSNPrs876658415
ebirs876658415
HLIrs876658415
Exacrs876658415
Varsomers876658415
Maprs876658415
PheGenIrs876658415
hapmaprs876658415
1000 genomesrs876658415
hgdprs876658415
ensemblrs876658415
gopubmedrs876658415
geneviewrs876658415
scholarrs876658415
googlers876658415
pharmgkbrs876658415
gwascentralrs876658415
openSNPrs876658415
23andMers876658415
23andMe allrs876658415
SNP Nexus

SNPshotrs876658415
SNPdbers876658415
MSV3drs876658415
GWAS Ctlgrs876658415
Max Magnitude0
ClinVar
Risk rs876658415(G;G)
Alt rs876658415(G;G)
Reference rs876658415(A;A)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene C11orf65 ATM
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000011.9:g.108186599A>G
CLNSRC
CLNACC RCV000216689.1,