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rs192810283

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs192810283(G;T)
Make rs192810283(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108271407
GeneATM
is asnp
is mentioned by
dbSNPrs192810283
ebirs192810283
HLIrs192810283
Exacrs192810283
Varsomers192810283
Maprs192810283
PheGenIrs192810283
hapmaprs192810283
1000 genomesrs192810283
hgdprs192810283
ensemblrs192810283
gopubmedrs192810283
geneviewrs192810283
scholarrs192810283
googlers192810283
pharmgkbrs192810283
gwascentralrs192810283
openSNPrs192810283
23andMers192810283
23andMe allrs192810283
SNP Nexus

SNPshotrs192810283
SNPdbers192810283
MSV3drs192810283
GWAS Ctlgrs192810283
Max Magnitude0
ClinVar
Risk rs192810283(A,T;A,T)
Alt rs192810283(A,T;A,T)
Reference rs192810283(G;G)
Significance Probable-Pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108142134G>A
CLNSRC
CLNACC RCV000206879.2,