rs1128977
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1128977(C;C) |
Make rs1128977(C;T) |
Make rs1128977(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 165419892 |
Gene | RXRG |
is a | snp |
is | mentioned by |
dbSNP | rs1128977 |
dbSNP (classic) | rs1128977 |
ClinGen | rs1128977 |
ebi | rs1128977 |
HLI | rs1128977 |
Exac | rs1128977 |
Gnomad | rs1128977 |
Varsome | rs1128977 |
LitVar | rs1128977 |
Map | rs1128977 |
PheGenI | rs1128977 |
Biobank | rs1128977 |
1000 genomes | rs1128977 |
hgdp | rs1128977 |
ensembl | rs1128977 |
geneview | rs1128977 |
scholar | rs1128977 |
rs1128977 | |
pharmgkb | rs1128977 |
gwascentral | rs1128977 |
openSNP | rs1128977 |
23andMe | rs1128977 |
SNPshot | rs1128977 |
SNPdbe | rs1128977 |
MSV3d | rs1128977 |
GWAS Ctlg | rs1128977 |
Merged from | Rs3818569 |
GMAF | 0.2392 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 18937358] Characteristics of a spina bifida population including North American Caucasian and Hispanic individuals.
[PMID 24222859] Association of RXR-Gamma Gene Variants with Familial Combined Hyperlipidemia: Genotype and Haplotype Analysis