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rs267606668

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs267606668(GC;GC)
Make rs267606668(GC;TG)
ReferenceGRCh38 38.1/141
Chromosome11
Position108332848
GeneATM
is asnp
is mentioned by
dbSNPrs267606668
ebirs267606668
HLIrs267606668
Exacrs267606668
Varsomers267606668
Maprs267606668
PheGenIrs267606668
hapmaprs267606668
1000 genomesrs267606668
hgdprs267606668
ensemblrs267606668
gopubmedrs267606668
geneviewrs267606668
scholarrs267606668
googlers267606668
pharmgkbrs267606668
gwascentralrs267606668
openSNPrs267606668
23andMers267606668
23andMe allrs267606668
SNP Nexus

SNPshotrs267606668
SNPdbers267606668
MSV3drs267606668
GWAS Ctlgrs267606668
Max Magnitude0
ClinVar
Risk rs267606668(GC;GC)
Alt rs267606668(GC;GC)
Reference rs267606668(TG;TG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108203575_108203576delTGinsGC
CLNSRC OMIM Allelic Variant
CLNACC RCV000132184.2, RCV000202436.1,