Have questions? Visit https://www.reddit.com/r/SNPedia

rs10508921

From SNPedia

Orientationplus
Stabilizedplus
Make rs10508921(C;C)
Make rs10508921(C;T)
Make rs10508921(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position50250948
is asnp
is mentioned by
dbSNPrs10508921
ebirs10508921
HLIrs10508921
Exacrs10508921
Varsomers10508921
Maprs10508921
PheGenIrs10508921
hapmaprs10508921
1000 genomesrs10508921
hgdprs10508921
ensemblrs10508921
gopubmedrs10508921
geneviewrs10508921
scholarrs10508921
googlers10508921
pharmgkbrs10508921
gwascentralrs10508921
openSNPrs10508921
23andMers10508921
23andMe allrs10508921
SNP Nexus

SNPshotrs10508921
SNPdbers10508921
MSV3drs10508921
GWAS Ctlgrs10508921
GMAF0.1625
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23400010OA-icon.png]
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 9E-7
Odds Ratio 25.70 [15.47-35.93] mg/dL decrease