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rs1060501711

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060501711(A;A)
Make rs1060501711(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position108279526
GeneATM
is asnp
is mentioned by
dbSNPrs1060501711
dbSNP (old)rs1060501711
ClinGenrs1060501711
ebirs1060501711
HLIrs1060501711
Exacrs1060501711
Gnomadrs1060501711
Varsomers1060501711
Maprs1060501711
PheGenIrs1060501711
Biobankrs1060501711
1000 genomesrs1060501711
hgdprs1060501711
ensemblrs1060501711
gopubmedrs1060501711
geneviewrs1060501711
scholarrs1060501711
googlers1060501711
pharmgkbrs1060501711
gwascentralrs1060501711
openSNPrs1060501711
23andMers1060501711
23andMe allrs1060501711
SNPshotrs1060501711
SNPdbers1060501711
MSV3drs1060501711
GWAS Ctlgrs1060501711
Max Magnitude0
ClinVar
Risk rs1060501711(A;A)
Alt rs1060501711(A;A)
Reference Rs1060501711(T;T)
Significance Pathogenic
Disease Ataxia-telangiectasia syndrome not provided
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108150253T>A
CLNSRC
CLNACC RCV000460640.1, RCV000485900.1,