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rs397514577

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397514577(A;A)
Make rs397514577(A;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position108317374
GeneATM
is asnp
is mentioned by
dbSNPrs397514577
ebirs397514577
HLIrs397514577
Exacrs397514577
Varsomers397514577
Maprs397514577
PheGenIrs397514577
hapmaprs397514577
1000 genomesrs397514577
hgdprs397514577
ensemblrs397514577
gopubmedrs397514577
geneviewrs397514577
scholarrs397514577
googlers397514577
pharmgkbrs397514577
gwascentralrs397514577
openSNPrs397514577
23andMers397514577
23andMe allrs397514577
SNP Nexus

SNPshotrs397514577
SNPdbers397514577
MSV3drs397514577
GWAS Ctlgrs397514577
Max Magnitude0
ClinVar
Risk rs397514577(A;A)
Alt rs397514577(A;A)
Reference rs397514577(C;C)
Significance Pathogenic
Disease Ataxia-telangiectasia variant Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Ataxia-telangiectasia variant Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108188101C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000032965.3, RCV000166627.1,