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rs676210

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs676210(A;A)
Make rs676210(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position21008652
GeneAPOB
is asnp
is mentioned by
dbSNPrs676210
ebirs676210
HLIrs676210
Exacrs676210
Varsomers676210
Maprs676210
PheGenIrs676210
hapmaprs676210
1000 genomesrs676210
hgdprs676210
ensemblrs676210
gopubmedrs676210
geneviewrs676210
scholarrs676210
googlers676210
pharmgkbrs676210
gwascentralrs676210
openSNPrs676210
23andMers676210
23andMe allrs676210
SNP Nexus

SNPshotrs676210
SNPdbers676210
MSV3drs676210
GWAS Ctlgrs676210
GMAF0.3379
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 20724655OA-icon.png] ApoB genetic variants modify the response to fenofibrate: a GOLDN study


[PMID 18296645OA-icon.png] Polymorphisms of genes in the lipid metabolism pathway and risk of biliary tract cancers and stones: a population-based case-control study in Shanghai, China.


[PMID 19474294OA-icon.png] Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.


[PMID 19936222OA-icon.png] Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.


GET Evidence
APOB-P2739L
aa_change Pro2739Leu
aa_change_short P2739L
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.197434
summary



[PMID 23247145] Genome-Wide Association Study Pinpoints a New Functional ApoB Variant Influencing Oxidized LDL Levels but Not Cardiovascular Events: AtheroRemo Consortium


[PMID 22715478] Genotypes associated with lipid metabolism contribute to differences in serum lipid profile of GH-deficient adults before and after GH replacement therapy.


ClinVar
Risk rs676210(A;A)
Alt rs676210(A;A)
Reference rs676210(G;G)
Significance Probable-non-pathogenic
Disease not specified
Variation info
Gene APOB
CLNDBN not specified
Reversed 0
HGVS NC_000002.11:g.21231524G>A
CLNSRC ClinVar University of Chicago
CLNACC RCV000116390.2,