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rs121434221

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Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121434221(A;G)
Make rs121434221(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position108329199
GeneATM
is asnp
is mentioned by
dbSNPrs121434221
ebirs121434221
HLIrs121434221
Exacrs121434221
Varsomers121434221
Maprs121434221
PheGenIrs121434221
hapmaprs121434221
1000 genomesrs121434221
hgdprs121434221
ensemblrs121434221
gopubmedrs121434221
geneviewrs121434221
scholarrs121434221
googlers121434221
pharmgkbrs121434221
gwascentralrs121434221
openSNPrs121434221
23andMers121434221
23andMe allrs121434221
SNP Nexus

SNPshotrs121434221
SNPdbers121434221
MSV3drs121434221
GWAS Ctlgrs121434221
Max Magnitude0
OMIM607585
Desc
Variant0022
Relatedalso
ClinVar
Risk rs121434221(G;G)
Alt rs121434221(G;G)
Reference rs121434221(A;A)
Significance Pathogenic
Disease Mantle cell lymphoma
Variation info
Gene C11orf65 ATM
CLNDBN Mantle cell lymphoma
Reversed 0
HGVS NC_000011.9:g.108199926A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000003180.3,