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rs794728018

From SNPedia

Orientationplus
Stabilizedplus
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
dbSNP (classic)rs794728018
ClinGenrs794728018
ebirs794728018
HLIrs794728018
Exacrs794728018
Gnomadrs794728018
Varsomers794728018
LitVarrs794728018
Maprs794728018
PheGenIrs794728018
Biobankrs794728018
1000 genomesrs794728018
hgdprs794728018
ensemblrs794728018
geneviewrs794728018
scholarrs794728018
googlers794728018
pharmgkbrs794728018
gwascentralrs794728018
openSNPrs794728018
23andMers794728018
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 Hereditary cancer-predisposing syndrome not specified
Variation info
Gene C11orf65 ATM
CLNDBN Breast cancer, early-onset Hereditary cancer-predisposing syndrome not specified
Reversed 0
HGVS NC_000011.9:g.108224553C>T
CLNSRC
CLNACC RCV000181011.1, RCV000214902.1, RCV000486041.1,