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rs876658716

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876658716(A;A)
Make rs876658716(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108345873
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs876658716
ebirs876658716
HLIrs876658716
Exacrs876658716
Varsomers876658716
Maprs876658716
PheGenIrs876658716
hapmaprs876658716
1000 genomesrs876658716
hgdprs876658716
ensemblrs876658716
gopubmedrs876658716
geneviewrs876658716
scholarrs876658716
googlers876658716
pharmgkbrs876658716
gwascentralrs876658716
openSNPrs876658716
23andMers876658716
23andMe allrs876658716
SNP Nexus

SNPshotrs876658716
SNPdbers876658716
MSV3drs876658716
GWAS Ctlgrs876658716
Max Magnitude0
ClinVar
Risk rs876658716(A;A)
Alt rs876658716(A;A)
Reference rs876658716(T;T)
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.108216600T>A
CLNSRC
CLNACC RCV000215215.1,