rs35463555
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs35463555(A;A) |
Make rs35463555(A;G) |
Make rs35463555(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 50374423 |
Gene | NR1H2 |
is a | snp |
is | mentioned by |
dbSNP | rs35463555 |
dbSNP (classic) | rs35463555 |
ClinGen | rs35463555 |
ebi | rs35463555 |
HLI | rs35463555 |
Exac | rs35463555 |
Gnomad | rs35463555 |
Varsome | rs35463555 |
LitVar | rs35463555 |
Map | rs35463555 |
PheGenI | rs35463555 |
Biobank | rs35463555 |
1000 genomes | rs35463555 |
hgdp | rs35463555 |
ensembl | rs35463555 |
geneview | rs35463555 |
scholar | rs35463555 |
rs35463555 | |
pharmgkb | rs35463555 |
gwascentral | rs35463555 |
openSNP | rs35463555 |
23andMe | rs35463555 |
SNPshot | rs35463555 |
SNPdbe | rs35463555 |
MSV3d | rs35463555 |
GWAS Ctlg | rs35463555 |
GMAF | 0.2691 |
Max Magnitude | 0 |
[PMID 19292929] Functional and genetic analysis in type 2 diabetes of Liver X receptor alleles - a cohort study.
[PMID 22029530] A common polymorphism in NR1H2 (LXRbeta) is associated with preeclampsia
[PMID 23838803] Association of liver X receptors (LXRs) genetic variants to gallbladder cancer susceptibility