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rs3092857

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs3092857(A;G)
Make rs3092857(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position108272572
GeneATM
is asnp
is mentioned by
dbSNPrs3092857
ebirs3092857
HLIrs3092857
Exacrs3092857
Varsomers3092857
Maprs3092857
PheGenIrs3092857
hapmaprs3092857
1000 genomesrs3092857
hgdprs3092857
ensemblrs3092857
gopubmedrs3092857
geneviewrs3092857
scholarrs3092857
googlers3092857
pharmgkbrs3092857
gwascentralrs3092857
openSNPrs3092857
23andMers3092857
23andMe allrs3092857
SNP Nexus

SNPshotrs3092857
SNPdbers3092857
MSV3drs3092857
GWAS Ctlgrs3092857
GMAF0.01102
Max Magnitude0
? (A;A) (A;G) (G;G) 28

NOTE: the OMIM entry cited below refers to a somatic mutation, not a germline SNP

OMIM607585
DescB-CELL NON-HODGKIN LYMPHOMA, SOMATIC
Variant0010
Relatedalso
Neighborrs1800057
Distance157


ClinVar
Risk rs3092857(G;G)
Alt rs3092857(G;G)
Reference rs3092857(A;A)
Significance Other
Disease B-cell non-Hodgkin lymphoma not specified Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Variation info
Gene ATM
CLNDBN B-cell non-Hodgkin lymphoma not specified Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108143299A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000003166.4, RCV000116423.3, RCV000123734.4, RCV000203947.1, RCV000224788.1,



GET Evidence
ATM-M1040V
aa_change Met1040Val
aa_change_short M1040V
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0131065
summary