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rs2083637

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0
Make rs2083637(C;C)
Make rs2083637(C;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position20007664
is asnp
is mentioned by
dbSNPrs2083637
ebirs2083637
HLIrs2083637
Exacrs2083637
Varsomers2083637
Maprs2083637
PheGenIrs2083637
hapmaprs2083637
1000 genomesrs2083637
hgdprs2083637
ensemblrs2083637
gopubmedrs2083637
geneviewrs2083637
scholarrs2083637
googlers2083637
pharmgkbrs2083637
gwascentralrs2083637
openSNPrs2083637
23andMers2083637
23andMe allrs2083637
SNP Nexus

SNPshotrs2083637
SNPdbers2083637
MSV3drs2083637
GWAS Ctlgrs2083637
GMAF0.2365
Max Magnitude0
? (C;C) (C;T) (T;T) 28

news three SNPs that appear to have different effects in men and women rs3846662 rs2304130 rs2083637

GWAS snp
PMID [PMID 19060911OA-icon.png]
Trait HDL cholesterol
Title Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts
Risk Allele G
P-val 6E-18
Odds Ratio 0.11 [NR] SD increase
GWAS snp
PMID [PMID 18454146]
Trait Waist circumference and related phenotypes
Title Common genetic variation near MC4R is associated with waist circumference and insulin resistance
Risk Allele
P-val 0.0000050000000000000004
Odds Ratio NR NR


OMIM609708
DescLIPOPROTEIN LIPASE; LPL
Variant
Relatedalso
GWAS snp
PMID [PMID 20694148OA-icon.png]
Trait
Title A genome-wide association study of the metabolic syndrome in Indian Asian men
Risk Allele G
P-val 2E-10
Odds Ratio 0.04 [0.02-0.05] mmol/l increase


[PMID 19041386OA-icon.png] Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review.


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


[PMID 20160193OA-icon.png] Investigation of variants identified in caucasian genome-wide association studies for plasma high-density lipoprotein cholesterol and triglycerides levels in Mexican dyslipidemic study samples.


[PMID 20502693OA-icon.png] Genetics and beyond--the transcriptome of human monocytes and disease susceptibility.


[PMID 21304891OA-icon.png] A study of CNVs as trait-associated polymorphisms and as expression quantitative trait loci.


GET Evidence
rs2083637
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.195312
summary



[PMID 25156894OA-icon.png] Lipoprotein lipase variants interact with polyunsaturated fatty acids for obesity traits in women: Replication in two populations