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rs876659365

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876659365(G;G)
Make rs876659365(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108330314
GeneATM
is asnp
is mentioned by
dbSNPrs876659365
ebirs876659365
HLIrs876659365
Exacrs876659365
Varsomers876659365
Maprs876659365
PheGenIrs876659365
hapmaprs876659365
1000 genomesrs876659365
hgdprs876659365
ensemblrs876659365
gopubmedrs876659365
geneviewrs876659365
scholarrs876659365
googlers876659365
pharmgkbrs876659365
gwascentralrs876659365
openSNPrs876659365
23andMers876659365
23andMe allrs876659365
SNP Nexus

SNPshotrs876659365
SNPdbers876659365
MSV3drs876659365
GWAS Ctlgrs876659365
Max Magnitude0
ClinVar
Risk rs876659365(G;G)
Alt rs876659365(G;G)
Reference rs876659365(T;T)
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.108201041T>G
CLNSRC
CLNACC RCV000220077.1,