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rs1057517226

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517226(C;C)
Make rs1057517226(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position108282709
GeneATM
is asnp
is mentioned by
dbSNPrs1057517226
dbSNP (old)rs1057517226
ClinGenrs1057517226
ebirs1057517226
HLIrs1057517226
Exacrs1057517226
Gnomadrs1057517226
Varsomers1057517226
Maprs1057517226
PheGenIrs1057517226
Biobankrs1057517226
1000 genomesrs1057517226
hgdprs1057517226
ensemblrs1057517226
gopubmedrs1057517226
geneviewrs1057517226
scholarrs1057517226
googlers1057517226
pharmgkbrs1057517226
gwascentralrs1057517226
openSNPrs1057517226
23andMers1057517226
23andMe allrs1057517226
SNPshotrs1057517226
SNPdbers1057517226
MSV3drs1057517226
GWAS Ctlgrs1057517226
Max Magnitude0
ClinVar
Risk rs1057517226(C;C)
Alt rs1057517226(C;C)
Reference Rs1057517226(G;G)
Significance Probable-Pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108153436G>C
CLNSRC
CLNACC RCV000410163.1,