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rs10892151

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs10892151(C;T)
Make rs10892151(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position117661016
GeneDSCAML1
is asnp
is mentioned by
dbSNPrs10892151
ebirs10892151
HLIrs10892151
Exacrs10892151
Varsomers10892151
Maprs10892151
PheGenIrs10892151
hapmaprs10892151
1000 genomesrs10892151
hgdprs10892151
ensemblrs10892151
gopubmedrs10892151
geneviewrs10892151
scholarrs10892151
googlers10892151
pharmgkbrs10892151
gwascentralrs10892151
openSNPrs10892151
23andMers10892151
23andMe allrs10892151
SNP Nexus

SNPshotrs10892151
SNPdbers10892151
MSV3drs10892151
GWAS Ctlgrs10892151
GMAF0.08035
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19074352OA-icon.png]
Trait Triglycerides
Title A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection
Risk Allele A
P-val 3E-29
Odds Ratio NR NR
OMIM107720
DescAPOLIPOPROTEIN C-III; APOC3
Variant
Relatedalso
[PMID 21939545OA-icon.png] Antiretroviral treatment-induced dyslipidemia in HIV-infected patients is influenced by the APOC3-related rs10892151 polymorphism


GET Evidence
rs10892151
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.117188
summary