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rs11077614

From SNPedia

Orientationplus
Stabilizedplus
Make rs11077614(A;A)
Make rs11077614(A;G)
Make rs11077614(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position72598490
GeneLINC00511
is asnp
is mentioned by
dbSNPrs11077614
ebirs11077614
HLIrs11077614
Exacrs11077614
Varsomers11077614
Maprs11077614
PheGenIrs11077614
hapmaprs11077614
1000 genomesrs11077614
hgdprs11077614
ensemblrs11077614
gopubmedrs11077614
geneviewrs11077614
scholarrs11077614
googlers11077614
pharmgkbrs11077614
gwascentralrs11077614
openSNPrs11077614
23andMers11077614
23andMe allrs11077614
SNP Nexus

SNPshotrs11077614
SNPdbers11077614
MSV3drs11077614
GWAS Ctlgrs11077614
GMAF0.359
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 3E-6
Odds Ratio 3.25 [1.92-4.58] mg/dL decrease