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rs6102059

From SNPedia

Orientationplus
Stabilizedplus
Make rs6102059(C;C)
Make rs6102059(C;T)
Make rs6102059(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position40600144
GeneLOC102724968
is asnp
is mentioned by
dbSNPrs6102059
ebirs6102059
HLIrs6102059
Exacrs6102059
Varsomers6102059
Maprs6102059
PheGenIrs6102059
hapmaprs6102059
1000 genomesrs6102059
hgdprs6102059
ensemblrs6102059
gopubmedrs6102059
geneviewrs6102059
scholarrs6102059
googlers6102059
pharmgkbrs6102059
gwascentralrs6102059
openSNPrs6102059
23andMers6102059
23andMe allrs6102059
SNP Nexus

SNPshotrs6102059
SNPdbers6102059
MSV3drs6102059
GWAS Ctlgrs6102059
GMAF0.3875
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19060906OA-icon.png]
Trait LDL cholesterol
Title Common variants at 30 loci contribute to polygenic dyslipidemia
Risk Allele T
P-val 4E-9
Odds Ratio 0.06 [0.03-0.10] SD decrease



[PMID 21738485OA-icon.png] Genetic determinants of lipid traits in diverse populations from the population architecture using genomics and epidemiology (PAGE) study


[PMID 19951432OA-icon.png] Analysis of recently identified dyslipidemia alleles reveals two loci that contribute to risk for carotid artery disease.


GET Evidence
rs6102059
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.34127
summary