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rs1057517358

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057517358(A;G)
Make rs1057517358(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position108252815
GeneATM
is asnp
is mentioned by
dbSNPrs1057517358
dbSNP (old)rs1057517358
ClinGenrs1057517358
ebirs1057517358
HLIrs1057517358
Exacrs1057517358
Gnomadrs1057517358
Varsomers1057517358
LitVarrs1057517358
Maprs1057517358
PheGenIrs1057517358
Biobankrs1057517358
1000 genomesrs1057517358
hgdprs1057517358
ensemblrs1057517358
gopubmedrs1057517358
geneviewrs1057517358
scholarrs1057517358
googlers1057517358
pharmgkbrs1057517358
gwascentralrs1057517358
openSNPrs1057517358
23andMers1057517358
23andMe allrs1057517358
SNPshotrs1057517358
SNPdbers1057517358
MSV3drs1057517358
GWAS Ctlgrs1057517358
Max Magnitude0
ClinVar
Risk rs1057517358(G;G)
Alt rs1057517358(G;G)
Reference Rs1057517358(A;A)
Significance Probable-Pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108123542A>G
CLNSRC
CLNACC RCV000411840.1,