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rs864622479

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864622479(G;T)
Make rs864622479(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108292770
GeneATM
is asnp
is mentioned by
dbSNPrs864622479
ebirs864622479
HLIrs864622479
Exacrs864622479
Varsomers864622479
Maprs864622479
PheGenIrs864622479
hapmaprs864622479
1000 genomesrs864622479
hgdprs864622479
ensemblrs864622479
gopubmedrs864622479
geneviewrs864622479
scholarrs864622479
googlers864622479
pharmgkbrs864622479
gwascentralrs864622479
openSNPrs864622479
23andMers864622479
23andMe allrs864622479
SNP Nexus

SNPshotrs864622479
SNPdbers864622479
MSV3drs864622479
GWAS Ctlgrs864622479
Max Magnitude0
ClinVar
Risk rs864622479(T;T)
Alt rs864622479(T;T)
Reference rs864622479(G;G)
Significance Pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108163497G>T
CLNSRC
CLNACC RCV000204978.1,