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rs121434223

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs121434223(C;G)
Make rs121434223(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position108301779
GeneATM
is asnp
is mentioned by
dbSNPrs121434223
ebirs121434223
HLIrs121434223
Exacrs121434223
Varsomers121434223
Maprs121434223
PheGenIrs121434223
hapmaprs121434223
1000 genomesrs121434223
hgdprs121434223
ensemblrs121434223
gopubmedrs121434223
geneviewrs121434223
scholarrs121434223
googlers121434223
pharmgkbrs121434223
gwascentralrs121434223
openSNPrs121434223
23andMers121434223
23andMe allrs121434223
SNP Nexus

SNPshotrs121434223
SNPdbers121434223
MSV3drs121434223
GWAS Ctlgrs121434223
Max Magnitude0
OMIM607585
Desc
Variant0025
Relatedalso
ClinVar
Risk rs121434223(G;G)
Alt rs121434223(G;G)
Reference rs121434223(C;C)
Significance Pathogenic
Disease T-cell prolymphocytic leukemia
Variation info
Gene ATM
CLNDBN T-cell prolymphocytic leukemia
Reversed 0
HGVS NC_000011.9:g.108172506C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000003183.6,