rs10918169
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10918169(C;C) |
Make rs10918169(C;G) |
Make rs10918169(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 165401238 |
Gene | RXRG |
is a | snp |
is | mentioned by |
dbSNP | rs10918169 |
dbSNP (classic) | rs10918169 |
ClinGen | rs10918169 |
ebi | rs10918169 |
HLI | rs10918169 |
Exac | rs10918169 |
Gnomad | rs10918169 |
Varsome | rs10918169 |
LitVar | rs10918169 |
Map | rs10918169 |
PheGenI | rs10918169 |
Biobank | rs10918169 |
1000 genomes | rs10918169 |
hgdp | rs10918169 |
ensembl | rs10918169 |
geneview | rs10918169 |
scholar | rs10918169 |
rs10918169 | |
pharmgkb | rs10918169 |
gwascentral | rs10918169 |
openSNP | rs10918169 |
23andMe | rs10918169 |
SNPshot | rs10918169 |
SNPdbe | rs10918169 |
MSV3d | rs10918169 |
GWAS Ctlg | rs10918169 |
GMAF | 0.1478 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 24222859] Association of RXR-Gamma Gene Variants with Familial Combined Hyperlipidemia: Genotype and Haplotype Analysis [PMID 18269685] Type 2 diabetes susceptibility genes on chromosome 1q21-24.