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rs1060501702

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060501702(-;-)
Make rs1060501702(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position108268546
GeneATM
is asnp
is mentioned by
dbSNPrs1060501702
dbSNP (old)rs1060501702
ClinGenrs1060501702
ebirs1060501702
HLIrs1060501702
Exacrs1060501702
Gnomadrs1060501702
Varsomers1060501702
Maprs1060501702
PheGenIrs1060501702
Biobankrs1060501702
1000 genomesrs1060501702
hgdprs1060501702
ensemblrs1060501702
gopubmedrs1060501702
geneviewrs1060501702
scholarrs1060501702
googlers1060501702
pharmgkbrs1060501702
gwascentralrs1060501702
openSNPrs1060501702
23andMers1060501702
23andMe allrs1060501702
SNPshotrs1060501702
SNPdbers1060501702
MSV3drs1060501702
GWAS Ctlgrs1060501702
Max Magnitude0
ClinVar
Risk rs1060501702(-;-)
Alt rs1060501702(-;-)
Reference Rs1060501702(G;G)
Significance Pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108139273delG
CLNSRC
CLNACC RCV000466879.1,