Have questions? Visit https://www.reddit.com/r/SNPedia

rs7770628

From SNPedia

Orientationplus
Stabilizedplus
Make rs7770628(C;C)
Make rs7770628(C;T)
Make rs7770628(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position160597142
GeneLPA
is asnp
is mentioned by
dbSNPrs7770628
ebirs7770628
HLIrs7770628
Exacrs7770628
Varsomers7770628
Maprs7770628
PheGenIrs7770628
hapmaprs7770628
1000 genomesrs7770628
hgdprs7770628
ensemblrs7770628
gopubmedrs7770628
geneviewrs7770628
scholarrs7770628
googlers7770628
pharmgkbrs7770628
gwascentralrs7770628
openSNPrs7770628
23andMers7770628
23andMe allrs7770628
SNP Nexus

SNPshotrs7770628
SNPdbers7770628
MSV3drs7770628
GWAS Ctlgrs7770628
GMAF0.2888
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS
SNP rs7770628
PubMedID [PMID 18464913OA-icon.png]
Condition Protein quantitative trait loci
Gene LPA
Risk Allele T
pValue 4.00E-010
OR NA
95% CI


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



GET Evidence
rs7770628
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.698413
summary