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rs7965364

From SNPedia

Orientationplus
Stabilizedplus
Make rs7965364(C;C)
Make rs7965364(C;T)
Make rs7965364(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position25331259
is asnp
is mentioned by
dbSNPrs7965364
dbSNP (classic)rs7965364
ClinGenrs7965364
ebirs7965364
HLIrs7965364
Exacrs7965364
Gnomadrs7965364
Varsomers7965364
LitVarrs7965364
Maprs7965364
PheGenIrs7965364
Biobankrs7965364
1000 genomesrs7965364
hgdprs7965364
ensemblrs7965364
geneviewrs7965364
scholarrs7965364
googlers7965364
pharmgkbrs7965364
gwascentralrs7965364
openSNPrs7965364
23andMers7965364
SNPshotrs7965364
SNPdbers7965364
MSV3drs7965364
GWAS Ctlgrs7965364
GMAF0.3122
Max Magnitude0
? (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 3.79 [2.14-5.44] mg/dL increase