{{Rsnum
|rsid=11191548
|Gene=NT5C2
|Chromosome=10
|position=104846178
|Orientation=plus
|GMAF=0.1345
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.9 | 13.3 | 85.8
| HCB | 8.8 | 40.9 | 50.4
| JPT | 7.1 | 40.7 | 52.2
| YRI | 0.0 | 2.7 | 97.3
| ASW | 0.0 | 7.0 | 93.0
| CHB | 8.8 | 40.9 | 50.4
| CHD | 8.3 | 43.1 | 48.6
| GIH | 6.0 | 38.0 | 56.0
| LWK | 0.0 | 4.5 | 95.5
| MEX | 3.6 | 28.6 | 67.9
| MKK | 0.0 | 8.3 | 91.7
| TSI | 0.0 | 22.8 | 77.2
| HapMapRevision=28
}}

{{PMID|19430483|OA=1
}}
[http://blog.23andme.com/2009/05/12/snpwatch-researchers-find-more-genetic-variations-associated-with-blood-pressure/ 23andMe blog] [[blood pressure]]

{{PMID Auto GWAS
|PMID=19430483
|Trait=Systolic blood pressure
|Title=Genome-wide association study identifies eight loci associated with blood pressure
|RiskAllele=T
|Pval=7E-24
|OR=1.16
|ORtxt=[0.92-1.40] mm Hg increase
|OA=1
}}

{{PMID Auto GWAS
|PMID=21572416
|Trait=None
|Title=Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians.
|RiskAllele=T
|Pval=4E-17
|OR=1.1800
|ORtxt=[0.91-1.45] mm Hg increase
|OA=1
}}

{{PMID Auto
|PMID=21963141
|Title=Genetic variations in CYP17A1, CACNB2 and PLEKHA7 are associated with blood pressure and/or hypertension in she ethnic minority of China
}}

{{PMID Auto GWAS
|PMID=21909115
|Trait=None
|Title=Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
|RiskAllele=T
|Pval=7E-26
|OR=1.0950
|ORtxt=[NR] mmHg increase
|OA=1
}}

{{PMID Auto GWAS
|PMID=21909110
|Trait=None
|Title=Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.
|RiskAllele=T
|Pval=8E-11
|OR=0.5290
|ORtxt=[0.37-0.69] mmHg increase
|OA=1
}}

{{PMID Auto
|PMID=20852445
|Title=Common variants in or near FGF5, CYP17A1 and MTHFR genes are associated with blood pressure and hypertension in Chinese Hans.
}}

{{PMID Auto
|PMID=22504314
|Title=Orthostatic hypotension and novel blood pressure-associated gene variants: Genetics of Postural Hemodynamics (GPH) Consortium.
|OA=1
}}

{{PMID Auto
|PMID=22525200
|Title=Pharmacogenetic implications for eight common blood pressure-associated single-nucleotide polymorphisms.
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs11191548
|overall_frequency_n=6
|overall_frequency_d=128
|overall_frequency=0.046875
|n_genomes=2
|n_genomes_annotated=0
|n_haplomes=3
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{PMID Auto
|PMID=23133444
|Title=Genetic variation in CYP17A1 is associated with arterial stiffness in diabetic subjects
|OA=1
}}

{{PMID Auto
|PMID=22048715
|Title=A sex-specific effect of the CYP17A1 SNP rs11191548 on blood pressure in Chinese children
}}

{{PMID Auto
|PMID=22959498
|Title=Recapitulation of four hypertension susceptibility genes (CSK, CYP17A1, MTHFR, and FGF5) in East Asians.
}}

{{PMID Auto
|PMID=23467202
|Title=Common polymorphism rs11191548 near the CYP17A1 gene is associated with hypertension and systolic blood pressure in the Han Chinese population.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}