rs10778699
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10778699(A;A) |
Make rs10778699(A;G) |
Make rs10778699(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 80069304 |
is a | snp |
is | mentioned by |
dbSNP | rs10778699 |
dbSNP (classic) | rs10778699 |
ClinGen | rs10778699 |
ebi | rs10778699 |
HLI | rs10778699 |
Exac | rs10778699 |
Gnomad | rs10778699 |
Varsome | rs10778699 |
LitVar | rs10778699 |
Map | rs10778699 |
PheGenI | rs10778699 |
Biobank | rs10778699 |
1000 genomes | rs10778699 |
hgdp | rs10778699 |
ensembl | rs10778699 |
geneview | rs10778699 |
scholar | rs10778699 |
rs10778699 | |
pharmgkb | rs10778699 |
gwascentral | rs10778699 |
openSNP | rs10778699 |
23andMe | rs10778699 |
SNPshot | rs10778699 |
SNPdbe | rs10778699 |
MSV3d | rs10778699 |
GWAS Ctlg | rs10778699 |
GMAF | 0.281 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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 | 4E-6 |
Odds Ratio | 4.28 [2.46-6.1] mg/dL increase |