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rs12307997

From SNPedia

Orientationplus
Stabilizedplus
Make rs12307997(A;A)
Make rs12307997(A;G)
Make rs12307997(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position7702675
is asnp
is mentioned by
dbSNPrs12307997
dbSNP (classic)rs12307997
ClinGenrs12307997
ebirs12307997
HLIrs12307997
Exacrs12307997
Gnomadrs12307997
Varsomers12307997
LitVarrs12307997
Maprs12307997
PheGenIrs12307997
Biobankrs12307997
1000 genomesrs12307997
hgdprs12307997
ensemblrs12307997
geneviewrs12307997
scholarrs12307997
googlers12307997
pharmgkbrs12307997
gwascentralrs12307997
openSNPrs12307997
23andMers12307997
SNPshotrs12307997
SNPdbers12307997
MSV3drs12307997
GWAS Ctlgrs12307997
GMAF0.169
Max Magnitude0
? (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 6E-7
Odds Ratio 22.11 [13.41-30.81] mg/dL increase