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rs1060501703

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060501703(A;G)
Make rs1060501703(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position108271062
GeneATM
is asnp
is mentioned by
dbSNPrs1060501703
dbSNP (old)rs1060501703
ClinGenrs1060501703
ebirs1060501703
HLIrs1060501703
Exacrs1060501703
Gnomadrs1060501703
Varsomers1060501703
Maprs1060501703
PheGenIrs1060501703
Biobankrs1060501703
1000 genomesrs1060501703
hgdprs1060501703
ensemblrs1060501703
gopubmedrs1060501703
geneviewrs1060501703
scholarrs1060501703
googlers1060501703
pharmgkbrs1060501703
gwascentralrs1060501703
openSNPrs1060501703
23andMers1060501703
23andMe allrs1060501703
SNPshotrs1060501703
SNPdbers1060501703
MSV3drs1060501703
GWAS Ctlgrs1060501703
Max Magnitude0
ClinVar
Risk rs1060501703(G;G)
Alt rs1060501703(G;G)
Reference Rs1060501703(A;A)
Significance Probable-Pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108141789A>G
CLNSRC
CLNACC RCV000464493.1,