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rs878853518

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs878853518(-;A)
Make rs878853518(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108301673
GeneATM
is asnp
is mentioned by
dbSNPrs878853518
dbSNP (classic)rs878853518
ClinGenrs878853518
ebirs878853518
HLIrs878853518
Exacrs878853518
Gnomadrs878853518
Varsomers878853518
LitVarrs878853518
Maprs878853518
PheGenIrs878853518
Biobankrs878853518
1000 genomesrs878853518
hgdprs878853518
ensemblrs878853518
geneviewrs878853518
scholarrs878853518
googlers878853518
pharmgkbrs878853518
gwascentralrs878853518
openSNPrs878853518
23andMers878853518
SNPshotrs878853518
SNPdbers878853518
MSV3drs878853518
GWAS Ctlgrs878853518
Max Magnitude0
ClinVar
Risk rs878853518(A;A)
Alt rs878853518(A;A)
Reference Rs878853518(-;-)
Significance Pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108172400dupA
CLNSRC
CLNACC RCV000231244.1,