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rs6919346

From SNPedia

Orientationplus
Stabilizedplus
Make rs6919346(C;C)
Make rs6919346(C;T)
Make rs6919346(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position160539327
GeneLPA
is asnp
is mentioned by
dbSNPrs6919346
ebirs6919346
HLIrs6919346
Exacrs6919346
Varsomers6919346
Maprs6919346
PheGenIrs6919346
hapmaprs6919346
1000 genomesrs6919346
hgdprs6919346
ensemblrs6919346
gopubmedrs6919346
geneviewrs6919346
scholarrs6919346
googlers6919346
pharmgkbrs6919346
gwascentralrs6919346
openSNPrs6919346
23andMers6919346
23andMe allrs6919346
SNP Nexus

SNPshotrs6919346
SNPdbers6919346
MSV3drs6919346
GWAS Ctlgrs6919346
GMAF0.0854
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19124843OA-icon.png]
Trait Plasma Lp (a) levels
Title Genome-wide association study of plasma Lp(a)levels Identifies multiple genes on chromosome 6q
Risk Allele
P-val 4E-11
Odds Ratio 0.66 [mg/dl decrease]



[PMID 21127300OA-icon.png] Genetic variation in LPAL2, LPA, and PLG predicts plasma lipoprotein(a) level and carotid artery disease risk.


[PMID 21283670OA-icon.png] Single-nucleotide polymorphisms in LPA explain most of the ancestry-specific variation in Lp(a) levels in African Americans.


[PMID 21305047OA-icon.png] Variation in LPA is associated with Lp(a) levels in three populations from the Third National Health and Nutrition Examination Survey.


GET Evidence
rs6919346
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.859375
summary