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rs11785622

From SNPedia

Orientationplus
Stabilizedplus
Make rs11785622(C;C)
Make rs11785622(C;T)
Make rs11785622(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position98305511
is asnp
is mentioned by
dbSNPrs11785622
ebirs11785622
HLIrs11785622
Exacrs11785622
Varsomers11785622
Maprs11785622
PheGenIrs11785622
hapmaprs11785622
1000 genomesrs11785622
hgdprs11785622
ensemblrs11785622
gopubmedrs11785622
geneviewrs11785622
scholarrs11785622
googlers11785622
pharmgkbrs11785622
gwascentralrs11785622
openSNPrs11785622
23andMers11785622
23andMe allrs11785622
SNP Nexus

SNPshotrs11785622
SNPdbers11785622
MSV3drs11785622
GWAS Ctlgrs11785622
GMAF0.1391
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 4E-6
Odds Ratio 7.21 [4.15-10.27] mg/dL decrease