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rs7557067

From SNPedia

Orientationplus
Stabilizedplus
Make rs7557067(A;A)
Make rs7557067(A;G)
Make rs7557067(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position20985339
is asnp
is mentioned by
dbSNPrs7557067
ebirs7557067
HLIrs7557067
Exacrs7557067
Varsomers7557067
Maprs7557067
PheGenIrs7557067
hapmaprs7557067
1000 genomesrs7557067
hgdprs7557067
ensemblrs7557067
gopubmedrs7557067
geneviewrs7557067
scholarrs7557067
googlers7557067
pharmgkbrs7557067
gwascentralrs7557067
openSNPrs7557067
23andMers7557067
23andMe allrs7557067
SNP Nexus

SNPshotrs7557067
SNPdbers7557067
MSV3drs7557067
GWAS Ctlgrs7557067
GMAF0.3476
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 9E-12
Odds Ratio 0.08 [0.04-0.12] SD decrease



[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.


GET Evidence
rs7557067
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.761905
summary