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rs1060501669

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060501669(A;A)
Make rs1060501669(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position108301719
GeneATM
is asnp
is mentioned by
dbSNPrs1060501669
dbSNP (old)rs1060501669
ClinGenrs1060501669
ebirs1060501669
HLIrs1060501669
Exacrs1060501669
Gnomadrs1060501669
Varsomers1060501669
Maprs1060501669
PheGenIrs1060501669
Biobankrs1060501669
1000 genomesrs1060501669
hgdprs1060501669
ensemblrs1060501669
gopubmedrs1060501669
geneviewrs1060501669
scholarrs1060501669
googlers1060501669
pharmgkbrs1060501669
gwascentralrs1060501669
openSNPrs1060501669
23andMers1060501669
23andMe allrs1060501669
SNPshotrs1060501669
SNPdbers1060501669
MSV3drs1060501669
GWAS Ctlgrs1060501669
Max Magnitude0
ClinVar
Risk rs1060501669(A;A)
Alt rs1060501669(A;A)
Reference Rs1060501669(G;G)
Significance Pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108172446G>A
CLNSRC
CLNACC RCV000470546.1,