rs1559759
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1559759(G;G) |
Make rs1559759(G;T) |
Make rs1559759(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 35101504 |
is a | snp |
is | mentioned by |
dbSNP | rs1559759 |
dbSNP (classic) | rs1559759 |
ClinGen | rs1559759 |
ebi | rs1559759 |
HLI | rs1559759 |
Exac | rs1559759 |
Gnomad | rs1559759 |
Varsome | rs1559759 |
LitVar | rs1559759 |
Map | rs1559759 |
PheGenI | rs1559759 |
Biobank | rs1559759 |
1000 genomes | rs1559759 |
hgdp | rs1559759 |
ensembl | rs1559759 |
geneview | rs1559759 |
scholar | rs1559759 |
rs1559759 | |
pharmgkb | rs1559759 |
gwascentral | rs1559759 |
openSNP | rs1559759 |
23andMe | rs1559759 |
SNPshot | rs1559759 |
SNPdbe | rs1559759 |
MSV3d | rs1559759 |
GWAS Ctlg | rs1559759 |
GMAF | 0.186 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23400010![]() |
Trait | Thiazide-induced adverse metabolic effects in hypertensive patients |
Title | Genome-wide association analyses suggest NELL1 influences adverse metabolic response to HCTZ in African Americans. |
Risk Allele | A |
P-val | 9E-6 |
Odds Ratio | 25.59 [14.3-36.88] mg/dL increase |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 11
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d