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rs121434217

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs121434217(C;C)
Make rs121434217(C;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position108299752
GeneATM
is asnp
is mentioned by
dbSNPrs121434217
ebirs121434217
HLIrs121434217
Exacrs121434217
Varsomers121434217
Maprs121434217
PheGenIrs121434217
hapmaprs121434217
1000 genomesrs121434217
hgdprs121434217
ensemblrs121434217
gopubmedrs121434217
geneviewrs121434217
scholarrs121434217
googlers121434217
pharmgkbrs121434217
gwascentralrs121434217
openSNPrs121434217
23andMers121434217
23andMe allrs121434217
SNP Nexus

SNPshotrs121434217
SNPdbers121434217
MSV3drs121434217
GWAS Ctlgrs121434217
Max Magnitude0
OMIM607585
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121434217(C;C)
Alt rs121434217(C;C)
Reference rs121434217(G;G)
Significance Pathogenic
Disease T-cell prolymphocytic leukemia
Variation info
Gene ATM
CLNDBN T-cell prolymphocytic leukemia
Reversed 0
HGVS NC_000011.9:g.108170479G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000003165.4,