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rs1060501677

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060501677(-;-)
Make rs1060501677(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position108272774
GeneATM
is asnp
is mentioned by
dbSNPrs1060501677
dbSNP (old)rs1060501677
ClinGenrs1060501677
ebirs1060501677
HLIrs1060501677
Exacrs1060501677
Gnomadrs1060501677
Varsomers1060501677
Maprs1060501677
PheGenIrs1060501677
Biobankrs1060501677
1000 genomesrs1060501677
hgdprs1060501677
ensemblrs1060501677
gopubmedrs1060501677
geneviewrs1060501677
scholarrs1060501677
googlers1060501677
pharmgkbrs1060501677
gwascentralrs1060501677
openSNPrs1060501677
23andMers1060501677
23andMe allrs1060501677
SNPshotrs1060501677
SNPdbers1060501677
MSV3drs1060501677
GWAS Ctlgrs1060501677
Max Magnitude0
ClinVar
Risk rs1060501677(-;-)
Alt rs1060501677(-;-)
Reference Rs1060501677(C;C)
Significance Pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108143501delC
CLNSRC
CLNACC RCV000463020.1,