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rs1057516876

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057516876(-;-)
Make rs1057516876(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position108251884
GeneATM
is asnp
is mentioned by
dbSNPrs1057516876
dbSNP (old)rs1057516876
ClinGenrs1057516876
ebirs1057516876
HLIrs1057516876
Exacrs1057516876
Gnomadrs1057516876
Varsomers1057516876
Maprs1057516876
PheGenIrs1057516876
Biobankrs1057516876
1000 genomesrs1057516876
hgdprs1057516876
ensemblrs1057516876
gopubmedrs1057516876
geneviewrs1057516876
scholarrs1057516876
googlers1057516876
pharmgkbrs1057516876
gwascentralrs1057516876
openSNPrs1057516876
23andMers1057516876
23andMe allrs1057516876
SNPshotrs1057516876
SNPdbers1057516876
MSV3drs1057516876
GWAS Ctlgrs1057516876
Max Magnitude0
ClinVar
Risk rs1057516876(-;-)
Alt rs1057516876(-;-)
Reference Rs1057516876(C;C)
Significance Probable-Pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108122611delC
CLNSRC
CLNACC RCV000411653.1,