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rs794728018

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728018(C;T)
Make rs794728018(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108353826
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs794728018
ebirs794728018
HLIrs794728018
Exacrs794728018
Varsomers794728018
Maprs794728018
PheGenIrs794728018
hapmaprs794728018
1000 genomesrs794728018
hgdprs794728018
ensemblrs794728018
gopubmedrs794728018
geneviewrs794728018
scholarrs794728018
googlers794728018
pharmgkbrs794728018
gwascentralrs794728018
openSNPrs794728018
23andMers794728018
23andMe allrs794728018
SNP Nexus

SNPshotrs794728018
SNPdbers794728018
MSV3drs794728018
GWAS Ctlgrs794728018
Max Magnitude0
ClinVar
Risk rs794728018(T;T)
Alt rs794728018(T;T)
Reference rs794728018(C;C)
Significance Pathogenic
Disease Breast cancer Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene C11orf65 ATM
CLNDBN Breast cancer, early-onset Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000011.9:g.108224553C>T
CLNSRC
CLNACC RCV000181011.1, RCV000214902.1,