Have questions? Visit https://www.reddit.com/r/SNPedia

rs876660066

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660066(A;A)
Make rs876660066(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108347278
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs876660066
ebirs876660066
HLIrs876660066
Exacrs876660066
Varsomers876660066
Maprs876660066
PheGenIrs876660066
hapmaprs876660066
1000 genomesrs876660066
hgdprs876660066
ensemblrs876660066
gopubmedrs876660066
geneviewrs876660066
scholarrs876660066
googlers876660066
pharmgkbrs876660066
gwascentralrs876660066
openSNPrs876660066
23andMers876660066
23andMe allrs876660066
SNP Nexus

SNPshotrs876660066
SNPdbers876660066
MSV3drs876660066
GWAS Ctlgrs876660066
Max Magnitude0
ClinVar
Risk rs876660066(A;A)
Alt rs876660066(A;A)
Reference rs876660066(G;G)
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.108218005G>A
CLNSRC
CLNACC RCV000217583.1,