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rs772926890

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs772926890(G;T)
Make rs772926890(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108251073
GeneATM
is asnp
is mentioned by
dbSNPrs772926890
ebirs772926890
HLIrs772926890
Exacrs772926890
Varsomers772926890
Maprs772926890
PheGenIrs772926890
hapmaprs772926890
1000 genomesrs772926890
hgdprs772926890
ensemblrs772926890
gopubmedrs772926890
geneviewrs772926890
scholarrs772926890
googlers772926890
pharmgkbrs772926890
gwascentralrs772926890
openSNPrs772926890
23andMers772926890
23andMe allrs772926890
SNP Nexus

SNPshotrs772926890
SNPdbers772926890
MSV3drs772926890
GWAS Ctlgrs772926890
Max Magnitude0
ClinVar
Risk rs772926890(T;T)
Alt rs772926890(T;T)
Reference rs772926890(G;G)
Significance Pathogenic
Disease Ataxia-telangiectasia syndrome not provided
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108121800G>T
CLNSRC
CLNACC RCV000203930.1, RCV000235749.1,