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rs10778699

From SNPedia

Orientationplus
Stabilizedplus
Make rs10778699(A;A)
Make rs10778699(A;G)
Make rs10778699(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position80069304
is asnp
is mentioned by
dbSNPrs10778699
ebirs10778699
HLIrs10778699
Exacrs10778699
Varsomers10778699
Maprs10778699
PheGenIrs10778699
hapmaprs10778699
1000 genomesrs10778699
hgdprs10778699
ensemblrs10778699
gopubmedrs10778699
geneviewrs10778699
scholarrs10778699
googlers10778699
pharmgkbrs10778699
gwascentralrs10778699
openSNPrs10778699
23andMers10778699
23andMe allrs10778699
SNP Nexus

SNPshotrs10778699
SNPdbers10778699
MSV3drs10778699
GWAS Ctlgrs10778699
GMAF0.281
Max Magnitude
? (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 A
P-val 4E-6
Odds Ratio 4.28 [2.46-6.1] mg/dL increase