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

rs121434222

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs121434222(C;T)
Make rs121434222(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position108287687
GeneATM
is asnp
is mentioned by
dbSNPrs121434222
ebirs121434222
HLIrs121434222
Exacrs121434222
Varsomers121434222
Maprs121434222
PheGenIrs121434222
hapmaprs121434222
1000 genomesrs121434222
hgdprs121434222
ensemblrs121434222
gopubmedrs121434222
geneviewrs121434222
scholarrs121434222
googlers121434222
pharmgkbrs121434222
gwascentralrs121434222
openSNPrs121434222
23andMers121434222
23andMe allrs121434222
SNP Nexus

SNPshotrs121434222
SNPdbers121434222
MSV3drs121434222
GWAS Ctlgrs121434222
Max Magnitude0
OMIM607585
Desc
Variant0024
Relatedalso
ClinVar
Risk rs121434222(T;T)
Alt rs121434222(T;T)
Reference rs121434222(C;C)
Significance Pathogenic
Disease Mantle cell lymphoma
Variation info
Gene ATM
CLNDBN Mantle cell lymphoma
Reversed 0
HGVS NC_000011.9:g.108158414C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003182.6,