rs2277862
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2277862(A;A) |
Make rs2277862(A;G) |
Make rs2277862(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 35564866 |
Gene | FER1L4 |
is a | snp |
is | mentioned by |
dbSNP | rs2277862 |
dbSNP (classic) | rs2277862 |
ClinGen | rs2277862 |
ebi | rs2277862 |
HLI | rs2277862 |
Exac | rs2277862 |
Gnomad | rs2277862 |
Varsome | rs2277862 |
LitVar | rs2277862 |
Map | rs2277862 |
PheGenI | rs2277862 |
Biobank | rs2277862 |
1000 genomes | rs2277862 |
hgdp | rs2277862 |
ensembl | rs2277862 |
geneview | rs2277862 |
scholar | rs2277862 |
rs2277862 | |
pharmgkb | rs2277862 |
gwascentral | rs2277862 |
openSNP | rs2277862 |
23andMe | rs2277862 |
SNPshot | rs2277862 |
SNPdbe | rs2277862 |
MSV3d | rs2277862 |
GWAS Ctlg | rs2277862 |
GMAF | 0.1474 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20686565] |
Trait | |
Title | Biological, clinical and population relevance of 95 loci for blood lipids. |
Risk Allele | T |
P-val | 4E-10 |
Odds Ratio | 1.1900 None |
GWAS snp | |
---|---|
PMID | [PMID 24097068] |
Trait | Cholesterol, total |
Title | Discovery and refinement of loci associated with lipid levels. |
Risk Allele | T |
P-val | 5E-11 |
Odds Ratio | .04 [NR] unit decrease |