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rs876658163

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876658163(C;T)
Make rs876658163(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108320003
GeneATM
is asnp
is mentioned by
dbSNPrs876658163
ebirs876658163
HLIrs876658163
Exacrs876658163
Varsomers876658163
Maprs876658163
PheGenIrs876658163
hapmaprs876658163
1000 genomesrs876658163
hgdprs876658163
ensemblrs876658163
gopubmedrs876658163
geneviewrs876658163
scholarrs876658163
googlers876658163
pharmgkbrs876658163
gwascentralrs876658163
openSNPrs876658163
23andMers876658163
23andMe allrs876658163
SNP Nexus

SNPshotrs876658163
SNPdbers876658163
MSV3drs876658163
GWAS Ctlgrs876658163
Max Magnitude0
ClinVar
Risk rs876658163(T;T)
Alt rs876658163(T;T)
Reference rs876658163(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.108190730C>T
CLNSRC
CLNACC RCV000219604.1,