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rs1060501599

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060501599(G;T)
Make rs1060501599(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position108253854
GeneATM
is asnp
is mentioned by
dbSNPrs1060501599
dbSNP (old)rs1060501599
ClinGenrs1060501599
ebirs1060501599
HLIrs1060501599
Exacrs1060501599
Gnomadrs1060501599
Varsomers1060501599
Maprs1060501599
PheGenIrs1060501599
Biobankrs1060501599
1000 genomesrs1060501599
hgdprs1060501599
ensemblrs1060501599
gopubmedrs1060501599
geneviewrs1060501599
scholarrs1060501599
googlers1060501599
pharmgkbrs1060501599
gwascentralrs1060501599
openSNPrs1060501599
23andMers1060501599
23andMe allrs1060501599
SNPshotrs1060501599
SNPdbers1060501599
MSV3drs1060501599
GWAS Ctlgrs1060501599
Max Magnitude0
ClinVar
Risk rs1060501599(T;T)
Alt rs1060501599(T;T)
Reference Rs1060501599(G;G)
Significance Pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108124581G>T
CLNSRC
CLNACC RCV000464991.1,