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rs1057517213

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057517213(A;G)
Make rs1057517213(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position108284225
GeneATM
is asnp
is mentioned by
dbSNPrs1057517213
dbSNP (classic)rs1057517213
ClinGenrs1057517213
ebirs1057517213
HLIrs1057517213
Exacrs1057517213
Gnomadrs1057517213
Varsomers1057517213
LitVarrs1057517213
Maprs1057517213
PheGenIrs1057517213
Biobankrs1057517213
1000 genomesrs1057517213
hgdprs1057517213
ensemblrs1057517213
geneviewrs1057517213
scholarrs1057517213
googlers1057517213
pharmgkbrs1057517213
gwascentralrs1057517213
openSNPrs1057517213
23andMers1057517213
SNPshotrs1057517213
SNPdbers1057517213
MSV3drs1057517213
GWAS Ctlgrs1057517213
Max Magnitude0
ClinVar
Risk rs1057517213(G;G)
Alt rs1057517213(G;G)
Reference Rs1057517213(A;A)
Significance Probable-Pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108154952A>G
CLNSRC
CLNACC RCV000409065.1,