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rs1060501687

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060501687(G;T)
Make rs1060501687(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position108272782
GeneATM
is asnp
is mentioned by
dbSNPrs1060501687
dbSNP (old)rs1060501687
ClinGenrs1060501687
ebirs1060501687
HLIrs1060501687
Exacrs1060501687
Gnomadrs1060501687
Varsomers1060501687
Maprs1060501687
PheGenIrs1060501687
Biobankrs1060501687
1000 genomesrs1060501687
hgdprs1060501687
ensemblrs1060501687
gopubmedrs1060501687
geneviewrs1060501687
scholarrs1060501687
googlers1060501687
pharmgkbrs1060501687
gwascentralrs1060501687
openSNPrs1060501687
23andMers1060501687
23andMe allrs1060501687
SNPshotrs1060501687
SNPdbers1060501687
MSV3drs1060501687
GWAS Ctlgrs1060501687
Max Magnitude0
ClinVar
Risk rs1060501687(T;T)
Alt rs1060501687(T;T)
Reference Rs1060501687(G;G)
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.108143509G>T
CLNSRC
CLNACC RCV000459347.1, RCV000478659.1,