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rs876658603

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876658603(-;-)
Make rs876658603(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108325394
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs876658603
dbSNP (old)rs876658603
ClinGenrs876658603
ebirs876658603
HLIrs876658603
Exacrs876658603
Gnomadrs876658603
Varsomers876658603
Maprs876658603
PheGenIrs876658603
Biobankrs876658603
1000 genomesrs876658603
hgdprs876658603
ensemblrs876658603
gopubmedrs876658603
geneviewrs876658603
scholarrs876658603
googlers876658603
pharmgkbrs876658603
gwascentralrs876658603
openSNPrs876658603
23andMers876658603
23andMe allrs876658603
SNP Nexus

SNPshotrs876658603
SNPdbers876658603
MSV3drs876658603
GWAS Ctlgrs876658603
Max Magnitude0
ClinVar
Risk rs876658603(-;-)
Alt rs876658603(-;-)
Reference Rs876658603(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108196121delT
CLNSRC
CLNACC RCV000218764.1,