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rs864622367

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs864622367(A;G)
Make rs864622367(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108319952
GeneATM
is asnp
is mentioned by
dbSNPrs864622367
ebirs864622367
HLIrs864622367
Exacrs864622367
Varsomers864622367
Maprs864622367
PheGenIrs864622367
hapmaprs864622367
1000 genomesrs864622367
hgdprs864622367
ensemblrs864622367
gopubmedrs864622367
geneviewrs864622367
scholarrs864622367
googlers864622367
pharmgkbrs864622367
gwascentralrs864622367
openSNPrs864622367
23andMers864622367
23andMe allrs864622367
SNP Nexus

SNPshotrs864622367
SNPdbers864622367
MSV3drs864622367
GWAS Ctlgrs864622367
Max Magnitude0
ClinVar
Risk rs864622367(G;G)
Alt rs864622367(G;G)
Reference rs864622367(A;A)
Significance Probable-Pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108190679A>G
CLNSRC
CLNACC RCV000204096.1,