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rs1060501692

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060501692(A;A)
Make rs1060501692(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position108288976
GeneATM
is asnp
is mentioned by
dbSNPrs1060501692
dbSNP (old)rs1060501692
ClinGenrs1060501692
ebirs1060501692
HLIrs1060501692
Exacrs1060501692
Gnomadrs1060501692
Varsomers1060501692
Maprs1060501692
PheGenIrs1060501692
Biobankrs1060501692
1000 genomesrs1060501692
hgdprs1060501692
ensemblrs1060501692
gopubmedrs1060501692
geneviewrs1060501692
scholarrs1060501692
googlers1060501692
pharmgkbrs1060501692
gwascentralrs1060501692
openSNPrs1060501692
23andMers1060501692
23andMe allrs1060501692
SNPshotrs1060501692
SNPdbers1060501692
MSV3drs1060501692
GWAS Ctlgrs1060501692
Max Magnitude0
ClinVar
Risk rs1060501692(A;A)
Alt rs1060501692(A;A)
Reference Rs1060501692(G;G)
Significance Pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108159703G>A
CLNSRC
CLNACC RCV000462992.1,