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rs7819412

From SNPedia

Orientationplus
Stabilizedplus
Make rs7819412(A;A)
Make rs7819412(A;G)
Make rs7819412(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position11187652
GeneXKR6
is asnp
is mentioned by
dbSNPrs7819412
ebirs7819412
HLIrs7819412
Exacrs7819412
Varsomers7819412
Maprs7819412
PheGenIrs7819412
hapmaprs7819412
1000 genomesrs7819412
hgdprs7819412
ensemblrs7819412
gopubmedrs7819412
geneviewrs7819412
scholarrs7819412
googlers7819412
pharmgkbrs7819412
gwascentralrs7819412
openSNPrs7819412
23andMers7819412
23andMe allrs7819412
SNP Nexus

SNPshotrs7819412
SNPdbers7819412
MSV3drs7819412
GWAS Ctlgrs7819412
GMAF0.4725
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19060906OA-icon.png]
Trait Triglycerides
Title Common variants at 30 loci contribute to polygenic dyslipidemia
Risk Allele G
P-val 3E-8
Odds Ratio 0.04 [0.001-0.08] SD decrease


[PMID 19364639OA-icon.png] The effect of a novel intergenic polymorphism (rs11774572) on HDL-cholesterol concentrations depends on TaqIB polymorphism in the cholesterol ester transfer protein gene.

[PMID 19936222OA-icon.png] Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.

[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 20421936OA-icon.png] Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups.


GET Evidence
rs7819412
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.563492
summary