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rs1060501642

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060501642(-;-)
Make rs1060501642(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position108244835
GeneATM
is asnp
is mentioned by
dbSNPrs1060501642
dbSNP (old)rs1060501642
ClinGenrs1060501642
ebirs1060501642
HLIrs1060501642
Exacrs1060501642
Gnomadrs1060501642
Varsomers1060501642
LitVarrs1060501642
Maprs1060501642
PheGenIrs1060501642
Biobankrs1060501642
1000 genomesrs1060501642
hgdprs1060501642
ensemblrs1060501642
gopubmedrs1060501642
geneviewrs1060501642
scholarrs1060501642
googlers1060501642
pharmgkbrs1060501642
gwascentralrs1060501642
openSNPrs1060501642
23andMers1060501642
23andMe allrs1060501642
SNPshotrs1060501642
SNPdbers1060501642
MSV3drs1060501642
GWAS Ctlgrs1060501642
Max Magnitude0
ClinVar
Risk rs1060501642(-;-)
Alt rs1060501642(-;-)
Reference Rs1060501642(C;C)
Significance Pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108115562delC
CLNSRC
CLNACC RCV000456893.1,