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rs876658455

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876658455(-;-)
Make rs876658455(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108282837
GeneATM
is asnp
is mentioned by
dbSNPrs876658455
dbSNP (old)rs876658455
ClinGenrs876658455
ebirs876658455
HLIrs876658455
Exacrs876658455
Gnomadrs876658455
Varsomers876658455
Maprs876658455
PheGenIrs876658455
Biobankrs876658455
1000 genomesrs876658455
hgdprs876658455
ensemblrs876658455
gopubmedrs876658455
geneviewrs876658455
scholarrs876658455
googlers876658455
pharmgkbrs876658455
gwascentralrs876658455
openSNPrs876658455
23andMers876658455
23andMe allrs876658455
SNP Nexus

SNPshotrs876658455
SNPdbers876658455
MSV3drs876658455
GWAS Ctlgrs876658455
Max Magnitude0
ClinVar
Risk rs876658455(-;-)
Alt rs876658455(-;-)
Reference Rs876658455(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108153564delC
CLNSRC
CLNACC RCV000219783.1,