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rs876658182

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658182(A;A)
Make rs876658182(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108345909
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs876658182
ebirs876658182
HLIrs876658182
Exacrs876658182
Varsomers876658182
Maprs876658182
PheGenIrs876658182
hapmaprs876658182
1000 genomesrs876658182
hgdprs876658182
ensemblrs876658182
gopubmedrs876658182
geneviewrs876658182
scholarrs876658182
googlers876658182
pharmgkbrs876658182
gwascentralrs876658182
openSNPrs876658182
23andMers876658182
23andMe allrs876658182
SNP Nexus

SNPshotrs876658182
SNPdbers876658182
MSV3drs876658182
GWAS Ctlgrs876658182
Max Magnitude0
ClinVar
Risk rs876658182(A;A)
Alt rs876658182(A;A)
Reference rs876658182(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.108216636G>A
CLNSRC
CLNACC RCV000213099.1,