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rs876660813

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876660813(-;-)
Make rs876660813(-;T)
Make rs876660813(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108353860
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs876660813
ebirs876660813
HLIrs876660813
Exacrs876660813
Varsomers876660813
Maprs876660813
PheGenIrs876660813
hapmaprs876660813
1000 genomesrs876660813
hgdprs876660813
ensemblrs876660813
gopubmedrs876660813
geneviewrs876660813
scholarrs876660813
googlers876660813
pharmgkbrs876660813
gwascentralrs876660813
openSNPrs876660813
23andMers876660813
23andMe allrs876660813
SNP Nexus

SNPshotrs876660813
SNPdbers876660813
MSV3drs876660813
GWAS Ctlgrs876660813
Max Magnitude0
ClinVar
Risk rs876660813(T;T)
Alt rs876660813(T;T)
Reference rs876660813(;)
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.108224587dupT
CLNSRC
CLNACC RCV000213336.1,