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rs377349459

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs377349459(A;A)
Make rs377349459(A;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position108332886
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs377349459
ebirs377349459
HLIrs377349459
Exacrs377349459
Varsomers377349459
Maprs377349459
PheGenIrs377349459
hapmaprs377349459
1000 genomesrs377349459
hgdprs377349459
ensemblrs377349459
gopubmedrs377349459
geneviewrs377349459
scholarrs377349459
googlers377349459
pharmgkbrs377349459
gwascentralrs377349459
openSNPrs377349459
23andMers377349459
23andMe allrs377349459
SNP Nexus

SNPshotrs377349459
SNPdbers377349459
MSV3drs377349459
GWAS Ctlgrs377349459
Max Magnitude0
ClinVar
Risk rs377349459(A;A)
Alt rs377349459(A;A)
Reference rs377349459(G;G)
Significance Other
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108203613G>A
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000129649.4, RCV000169621.2, RCV000212077.1,