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

rs4635554

From SNPedia

Orientationplus
Stabilizedplus
Make rs4635554(G;G)
Make rs4635554(G;T)
Make rs4635554(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position21166787
is asnp
is mentioned by
dbSNPrs4635554
ebirs4635554
HLIrs4635554
Exacrs4635554
Varsomers4635554
Maprs4635554
PheGenIrs4635554
hapmaprs4635554
1000 genomesrs4635554
hgdprs4635554
ensemblrs4635554
gopubmedrs4635554
geneviewrs4635554
scholarrs4635554
googlers4635554
pharmgkbrs4635554
gwascentralrs4635554
openSNPrs4635554
23andMers4635554
23andMe allrs4635554
SNP Nexus

SNPshotrs4635554
SNPdbers4635554
MSV3drs4635554
GWAS Ctlgrs4635554
GMAF0.393
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 20657596OA-icon.png]
Trait Hypertriglyceridemia
Title Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia
Risk Allele G
P-val 2E-7
Odds Ratio 1.67 [1.38-2.02]