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rs1060499601

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060499601(-;-)
Make rs1060499601(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position108244913
GeneATM
is asnp
is mentioned by
dbSNPrs1060499601
dbSNP (old)rs1060499601
ClinGenrs1060499601
ebirs1060499601
HLIrs1060499601
Exacrs1060499601
Gnomadrs1060499601
Varsomers1060499601
Maprs1060499601
PheGenIrs1060499601
Biobankrs1060499601
1000 genomesrs1060499601
hgdprs1060499601
ensemblrs1060499601
gopubmedrs1060499601
geneviewrs1060499601
scholarrs1060499601
googlers1060499601
pharmgkbrs1060499601
gwascentralrs1060499601
openSNPrs1060499601
23andMers1060499601
23andMe allrs1060499601
SNPshotrs1060499601
SNPdbers1060499601
MSV3drs1060499601
GWAS Ctlgrs1060499601
Max Magnitude0
ClinVar
Risk rs1060499601(-;-)
Alt rs1060499601(-;-)
Reference Rs1060499601(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108115642delT
CLNSRC
CLNACC RCV000130373.3, RCV000233840.3, RCV000235917.2,