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

rs1800590

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs1800590(G;G)
Make rs1800590(G;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position19939160
GeneLPL
is asnp
is mentioned by
dbSNPrs1800590
dbSNP (classic)rs1800590
ClinGenrs1800590
ebirs1800590
HLIrs1800590
Exacrs1800590
Gnomadrs1800590
Varsomers1800590
LitVarrs1800590
Maprs1800590
PheGenIrs1800590
Biobankrs1800590
1000 genomesrs1800590
hgdprs1800590
ensemblrs1800590
geneviewrs1800590
scholarrs1800590
googlers1800590
pharmgkbrs1800590
gwascentralrs1800590
openSNPrs1800590
23andMers1800590
SNPshotrs1800590
SNPdbers1800590
MSV3drs1800590
GWAS Ctlgrs1800590
GMAF0.1061
Max Magnitude0

[PMID 27569544OA-icon.png] A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease. This SNP maps to a position listed in Table S6 as a non-coding variant that their biocurators felt was convincingly associated with a Mendelian disease.

? (G;G) (G;T) (T;T) 28


[PMID 19629056OA-icon.png] Apolipoprotein A5 and Lipoprotein Lipase Interact to Modulate Anthropometric Measures in Hispanics of Caribbean Origin


[PMID 18513389OA-icon.png] New application of intelligent agents in sporadic amyotrophic lateral sclerosis identifies unexpected specific genetic background.


[PMID 18922999] Seven lipoprotein lipase gene polymorphisms, lipid fractions, and coronary disease: a HuGE association review and meta-analysis.


[PMID 19131662OA-icon.png] A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients.


[PMID 23298194OA-icon.png] Epistatic study reveals two genetic interactions in blood pressure regulation


ClinVar
Risk rs1800590(G;G)
Alt rs1800590(G;G)
Reference Rs1800590(T;T)
Significance Non-pathogenic
Disease Hyperlipoproteinemia
Variation info
Gene LPL
CLNDBN Hyperlipoproteinemia, type I
Reversed 0
HGVS NC_000008.10:g.19796671T>G
CLNSRC
CLNACC RCV000326637.1,