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rs866521873

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs866521873(C;T)
Make rs866521873(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108250705
GeneATM
is asnp
is mentioned by
dbSNPrs866521873
ebirs866521873
HLIrs866521873
Exacrs866521873
Varsomers866521873
Maprs866521873
PheGenIrs866521873
hapmaprs866521873
1000 genomesrs866521873
hgdprs866521873
ensemblrs866521873
gopubmedrs866521873
geneviewrs866521873
scholarrs866521873
googlers866521873
pharmgkbrs866521873
gwascentralrs866521873
openSNPrs866521873
23andMers866521873
23andMe allrs866521873
SNP Nexus

SNPshotrs866521873
SNPdbers866521873
MSV3drs866521873
GWAS Ctlgrs866521873
Max Magnitude0
ClinVar
Risk rs866521873(A,T;A,T)
Alt rs866521873(A,T;A,T)
Reference rs866521873(C;C)
Significance Pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108121432C>T
CLNSRC
CLNACC RCV000230144.1,