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rs1060501627

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060501627(C;T)
Make rs1060501627(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position108295056
GeneATM
is asnp
is mentioned by
dbSNPrs1060501627
dbSNP (old)rs1060501627
ClinGenrs1060501627
ebirs1060501627
HLIrs1060501627
Exacrs1060501627
Gnomadrs1060501627
Varsomers1060501627
Maprs1060501627
PheGenIrs1060501627
Biobankrs1060501627
1000 genomesrs1060501627
hgdprs1060501627
ensemblrs1060501627
gopubmedrs1060501627
geneviewrs1060501627
scholarrs1060501627
googlers1060501627
pharmgkbrs1060501627
gwascentralrs1060501627
openSNPrs1060501627
23andMers1060501627
23andMe allrs1060501627
SNPshotrs1060501627
SNPdbers1060501627
MSV3drs1060501627
GWAS Ctlgrs1060501627
Max Magnitude0
ClinVar
Risk rs1060501627(T;T)
Alt rs1060501627(T;T)
Reference Rs1060501627(C;C)
Significance Pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108165783C>T
CLNSRC
CLNACC RCV000456566.1,