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rs876659489

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876659489(A;C)
Make rs876659489(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108310158
GeneATM
is asnp
is mentioned by
dbSNPrs876659489
ebirs876659489
HLIrs876659489
Exacrs876659489
Varsomers876659489
Maprs876659489
PheGenIrs876659489
hapmaprs876659489
1000 genomesrs876659489
hgdprs876659489
ensemblrs876659489
gopubmedrs876659489
geneviewrs876659489
scholarrs876659489
googlers876659489
pharmgkbrs876659489
gwascentralrs876659489
openSNPrs876659489
23andMers876659489
23andMe allrs876659489
SNP Nexus

SNPshotrs876659489
SNPdbers876659489
MSV3drs876659489
GWAS Ctlgrs876659489
Max Magnitude0
ClinVar
Risk rs876659489(C;C)
Alt rs876659489(C;C)
Reference rs876659489(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.108180885A>C
CLNSRC
CLNACC RCV000216373.1,