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rs1057516238

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057516238(G;T)
Make rs1057516238(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position108287599
GeneATM
is asnp
is mentioned by
dbSNPrs1057516238
dbSNP (old)rs1057516238
ClinGenrs1057516238
ebirs1057516238
HLIrs1057516238
Exacrs1057516238
Gnomadrs1057516238
Varsomers1057516238
Maprs1057516238
PheGenIrs1057516238
Biobankrs1057516238
1000 genomesrs1057516238
hgdprs1057516238
ensemblrs1057516238
gopubmedrs1057516238
geneviewrs1057516238
scholarrs1057516238
googlers1057516238
pharmgkbrs1057516238
gwascentralrs1057516238
openSNPrs1057516238
23andMers1057516238
23andMe allrs1057516238
SNPshotrs1057516238
SNPdbers1057516238
MSV3drs1057516238
GWAS Ctlgrs1057516238
Max Magnitude0
ClinVar
Risk rs1057516238(T;T)
Alt rs1057516238(T;T)
Reference Rs1057516238(G;G)
Significance Probable-Pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108158326G>T
CLNSRC
CLNACC RCV000411542.1,