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rs876658394

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876658394(-;-)
Make rs876658394(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108325462
GeneATM
is asnp
is mentioned by
dbSNPrs876658394
ebirs876658394
HLIrs876658394
Exacrs876658394
Varsomers876658394
Maprs876658394
PheGenIrs876658394
hapmaprs876658394
1000 genomesrs876658394
hgdprs876658394
ensemblrs876658394
gopubmedrs876658394
geneviewrs876658394
scholarrs876658394
googlers876658394
pharmgkbrs876658394
gwascentralrs876658394
openSNPrs876658394
23andMers876658394
23andMe allrs876658394
SNP Nexus

SNPshotrs876658394
SNPdbers876658394
MSV3drs876658394
GWAS Ctlgrs876658394
Max Magnitude0
ClinVar
Risk rs876658394(;)
Alt rs876658394(;)
Reference rs876658394(C;C)
Significance 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.108196189delC
CLNSRC
CLNACC RCV000219311.1,