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rs16951120

From SNPedia

Orientationplus
Stabilizedplus
Make rs16951120(C;C)
Make rs16951120(C;T)
Make rs16951120(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position52216278
is asnp
is mentioned by
dbSNPrs16951120
ebirs16951120
HLIrs16951120
Exacrs16951120
Varsomers16951120
Maprs16951120
PheGenIrs16951120
hapmaprs16951120
1000 genomesrs16951120
hgdprs16951120
ensemblrs16951120
gopubmedrs16951120
geneviewrs16951120
scholarrs16951120
googlers16951120
pharmgkbrs16951120
gwascentralrs16951120
openSNPrs16951120
23andMers16951120
23andMe allrs16951120
SNP Nexus

SNPshotrs16951120
SNPdbers16951120
MSV3drs16951120
GWAS Ctlgrs16951120
GMAF0.1129
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 6E-6
Odds Ratio 4.49 [2.55-6.43] mg/dL increase