Have questions? Visit https://www.reddit.com/r/SNPedia

rs878853490

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878853490(-;-)
Make rs878853490(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108229184
GeneATM
is asnp
is mentioned by
dbSNPrs878853490
ebirs878853490
HLIrs878853490
Exacrs878853490
Varsomers878853490
Maprs878853490
PheGenIrs878853490
hapmaprs878853490
1000 genomesrs878853490
hgdprs878853490
ensemblrs878853490
gopubmedrs878853490
geneviewrs878853490
scholarrs878853490
googlers878853490
pharmgkbrs878853490
gwascentralrs878853490
openSNPrs878853490
23andMers878853490
23andMe allrs878853490
SNP Nexus

SNPshotrs878853490
SNPdbers878853490
MSV3drs878853490
GWAS Ctlgrs878853490
Max Magnitude0
ClinVar
Risk rs878853490(;)
Alt rs878853490(;)
Reference rs878853490(A;A)
Significance Pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108099911delA
CLNSRC
CLNACC RCV000231922.1,