Have questions? Visit https://www.reddit.com/r/SNPedia

rs1060499600

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060499600(-;-)
Make rs1060499600(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position108244947
GeneATM
is asnp
is mentioned by
dbSNPrs1060499600
dbSNP (old)rs1060499600
ClinGenrs1060499600
ebirs1060499600
HLIrs1060499600
Exacrs1060499600
Gnomadrs1060499600
Varsomers1060499600
LitVarrs1060499600
Maprs1060499600
PheGenIrs1060499600
Biobankrs1060499600
1000 genomesrs1060499600
hgdprs1060499600
ensemblrs1060499600
gopubmedrs1060499600
geneviewrs1060499600
scholarrs1060499600
googlers1060499600
pharmgkbrs1060499600
gwascentralrs1060499600
openSNPrs1060499600
23andMers1060499600
23andMe allrs1060499600
SNPshotrs1060499600
SNPdbers1060499600
MSV3drs1060499600
GWAS Ctlgrs1060499600
Max Magnitude0
ClinVar
Risk rs1060499600(-;-)
Alt rs1060499600(-;-)
Reference Rs1060499600(T;T)
Significance Pathogenic
Disease Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108115676delT
CLNSRC
CLNACC RCV000205636.2, RCV000221322.2,