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rs1060501528

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060501528(G;T)
Make rs1060501528(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position108287642
GeneATM
is asnp
is mentioned by
dbSNPrs1060501528
dbSNP (classic)rs1060501528
ClinGenrs1060501528
ebirs1060501528
HLIrs1060501528
Exacrs1060501528
Gnomadrs1060501528
Varsomers1060501528
LitVarrs1060501528
Maprs1060501528
PheGenIrs1060501528
Biobankrs1060501528
1000 genomesrs1060501528
hgdprs1060501528
ensemblrs1060501528
geneviewrs1060501528
scholarrs1060501528
googlers1060501528
pharmgkbrs1060501528
gwascentralrs1060501528
openSNPrs1060501528
23andMers1060501528
SNPshotrs1060501528
SNPdbers1060501528
MSV3drs1060501528
GWAS Ctlgrs1060501528
Max Magnitude0
ClinVar
Risk rs1060501528(T;T)
Alt rs1060501528(T;T)
Reference Rs1060501528(G;G)
Significance Pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108158369G>T
CLNSRC
CLNACC RCV000461052.1,