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rs7964748

From SNPedia

Orientationplus
Stabilizedplus
Make rs7964748(A;A)
Make rs7964748(A;G)
Make rs7964748(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position102571551
GeneLOC105369944
is asnp
is mentioned by
dbSNPrs7964748
dbSNP (classic)rs7964748
ClinGenrs7964748
ebirs7964748
HLIrs7964748
Exacrs7964748
Gnomadrs7964748
Varsomers7964748
LitVarrs7964748
Maprs7964748
PheGenIrs7964748
Biobankrs7964748
1000 genomesrs7964748
hgdprs7964748
ensemblrs7964748
geneviewrs7964748
scholarrs7964748
googlers7964748
pharmgkbrs7964748
gwascentralrs7964748
openSNPrs7964748
23andMers7964748
SNPshotrs7964748
SNPdbers7964748
MSV3drs7964748
GWAS Ctlgrs7964748
GMAF0.2176
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 3E-6
Odds Ratio 4.06 [2.37-5.75] mg/dL increase