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

rs1501908

From SNPedia

Orientationminus
Stabilizedminus
Make rs1501908(C;C)
Make rs1501908(C;G)
Make rs1501908(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position156971158
is asnp
is mentioned by
dbSNPrs1501908
ebirs1501908
HLIrs1501908
Exacrs1501908
Varsomers1501908
Maprs1501908
PheGenIrs1501908
hapmaprs1501908
1000 genomesrs1501908
hgdprs1501908
ensemblrs1501908
gopubmedrs1501908
geneviewrs1501908
scholarrs1501908
googlers1501908
pharmgkbrs1501908
gwascentralrs1501908
openSNPrs1501908
23andMers1501908
23andMe allrs1501908
SNP Nexus

SNPshotrs1501908
SNPdbers1501908
MSV3drs1501908
GWAS Ctlgrs1501908
GMAF0.3843
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 19060906OA-icon.png]
Trait LDL cholesterol
Title Common variants at 30 loci contribute to polygenic dyslipidemia
Risk Allele G
P-val 1E-11
Odds Ratio 0.07 [0.03-0.11] SD decrease



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


GET Evidence
rs1501908
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.59375
summary