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rs2274788

From SNPedia

Orientationplus
Stabilizedplus
Make rs2274788(C;C)
Make rs2274788(C;T)
Make rs2274788(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position94209170
GeneARHGAP29
is asnp
is mentioned by
dbSNPrs2274788
ebirs2274788
HLIrs2274788
Exacrs2274788
Varsomers2274788
Maprs2274788
PheGenIrs2274788
hapmaprs2274788
1000 genomesrs2274788
hgdprs2274788
ensemblrs2274788
gopubmedrs2274788
geneviewrs2274788
scholarrs2274788
googlers2274788
pharmgkbrs2274788
gwascentralrs2274788
openSNPrs2274788
23andMers2274788
23andMe allrs2274788
SNP Nexus

SNPshotrs2274788
SNPdbers2274788
MSV3drs2274788
GWAS Ctlgrs2274788
GMAF0.208
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 C
P-val 1E-6
Odds Ratio 23.07 [13.8-32.34] mg/dL decrease