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rs864622490

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864622490(A;A)
Make rs864622490(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108282796
GeneATM
is asnp
is mentioned by
dbSNPrs864622490
ebirs864622490
HLIrs864622490
Exacrs864622490
Varsomers864622490
Maprs864622490
PheGenIrs864622490
hapmaprs864622490
1000 genomesrs864622490
hgdprs864622490
ensemblrs864622490
gopubmedrs864622490
geneviewrs864622490
scholarrs864622490
googlers864622490
pharmgkbrs864622490
gwascentralrs864622490
openSNPrs864622490
23andMers864622490
23andMe allrs864622490
SNP Nexus

SNPshotrs864622490
SNPdbers864622490
MSV3drs864622490
GWAS Ctlgrs864622490
Max Magnitude0
ClinVar
Risk rs864622490(A;A)
Alt rs864622490(A;A)
Reference rs864622490(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.108153523G>A
CLNSRC
CLNACC RCV000206039.2, RCV000235543.1,