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rs7077606

From SNPedia

Orientationplus
Stabilizedplus
Make rs7077606(C;C)
Make rs7077606(C;T)
Make rs7077606(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position53647331
is asnp
is mentioned by
dbSNPrs7077606
ebirs7077606
HLIrs7077606
Exacrs7077606
Varsomers7077606
Maprs7077606
PheGenIrs7077606
hapmaprs7077606
1000 genomesrs7077606
hgdprs7077606
ensemblrs7077606
gopubmedrs7077606
geneviewrs7077606
scholarrs7077606
googlers7077606
pharmgkbrs7077606
gwascentralrs7077606
openSNPrs7077606
23andMers7077606
23andMe allrs7077606
SNP Nexus

SNPshotrs7077606
SNPdbers7077606
MSV3drs7077606
GWAS Ctlgrs7077606
GMAF0.1543
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 5E-7
Odds Ratio 5.44 [3.32-7.56] mg/dL decrease