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rs12507634

From SNPedia

Orientationplus
Stabilizedplus
Make rs12507634(A;A)
Make rs12507634(A;G)
Make rs12507634(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position174150451
is asnp
is mentioned by
dbSNPrs12507634
ebirs12507634
HLIrs12507634
Exacrs12507634
Varsomers12507634
Maprs12507634
PheGenIrs12507634
hapmaprs12507634
1000 genomesrs12507634
hgdprs12507634
ensemblrs12507634
gopubmedrs12507634
geneviewrs12507634
scholarrs12507634
googlers12507634
pharmgkbrs12507634
gwascentralrs12507634
openSNPrs12507634
23andMers12507634
23andMe allrs12507634
SNP Nexus

SNPshotrs12507634
SNPdbers12507634
MSV3drs12507634
GWAS Ctlgrs12507634
GMAF0.2879
Max Magnitude
? (A;A) (A;G) (G;G) 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 G
P-val 4E-6
Odds Ratio 4.84 [2.78-6.9] mg/dL decrease