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rs1779876

From SNPedia

Orientationplus
Stabilizedplus
Make rs1779876(G;G)
Make rs1779876(G;T)
Make rs1779876(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position36359112
is asnp
is mentioned by
dbSNPrs1779876
ebirs1779876
HLIrs1779876
Exacrs1779876
Varsomers1779876
Maprs1779876
PheGenIrs1779876
hapmaprs1779876
1000 genomesrs1779876
hgdprs1779876
ensemblrs1779876
gopubmedrs1779876
geneviewrs1779876
scholarrs1779876
googlers1779876
pharmgkbrs1779876
gwascentralrs1779876
openSNPrs1779876
23andMers1779876
23andMe allrs1779876
SNP Nexus

SNPshotrs1779876
SNPdbers1779876
MSV3drs1779876
GWAS Ctlgrs1779876
GMAF0.1543
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 18464913OA-icon.png]
Trait Protein quantitative trait loci
Title A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)
Risk Allele
P-val 0.0000030000000000000001
Odds Ratio NR NR

[PMID 18464913OA-icon.png] Lipoprotein A (LPA) protein levels


GET Evidence
rs1779876
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.148438
summary