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rs764389018

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs764389018(C;T)
Make rs764389018(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108301658
GeneATM
is asnp
is mentioned by
dbSNPrs764389018
ebirs764389018
HLIrs764389018
Exacrs764389018
Varsomers764389018
Maprs764389018
PheGenIrs764389018
hapmaprs764389018
1000 genomesrs764389018
hgdprs764389018
ensemblrs764389018
gopubmedrs764389018
geneviewrs764389018
scholarrs764389018
googlers764389018
pharmgkbrs764389018
gwascentralrs764389018
openSNPrs764389018
23andMers764389018
23andMe allrs764389018
SNP Nexus

SNPshotrs764389018
SNPdbers764389018
MSV3drs764389018
GWAS Ctlgrs764389018
Max Magnitude0
ClinVar
Risk rs764389018(T;T)
Alt rs764389018(T;T)
Reference rs764389018(C;C)
Significance Other
Disease Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108172385C>T
CLNSRC
CLNACC RCV000169451.2,