rs16951120
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs16951120(C;C) |
Make rs16951120(C;T) |
Make rs16951120(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 52216278 |
is a | snp |
is | mentioned by |
dbSNP | rs16951120 |
dbSNP (classic) | rs16951120 |
ClinGen | rs16951120 |
ebi | rs16951120 |
HLI | rs16951120 |
Exac | rs16951120 |
Gnomad | rs16951120 |
Varsome | rs16951120 |
LitVar | rs16951120 |
Map | rs16951120 |
PheGenI | rs16951120 |
Biobank | rs16951120 |
1000 genomes | rs16951120 |
hgdp | rs16951120 |
ensembl | rs16951120 |
geneview | rs16951120 |
scholar | rs16951120 |
rs16951120 | |
pharmgkb | rs16951120 |
gwascentral | rs16951120 |
openSNP | rs16951120 |
23andMe | rs16951120 |
SNPshot | rs16951120 |
SNPdbe | rs16951120 |
MSV3d | rs16951120 |
GWAS Ctlg | rs16951120 |
GMAF | 0.1129 |
Max Magnitude | 0 |
? | (C;C) (C;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 | T |
P-val | 6E-6 |
Odds Ratio | 4.49 [2.55-6.43] mg/dL increase |