rs11191548

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Geno	Mag	Summary
(T;T)	0

Make rs11191548(C;C)

Make rs11191548(C;T)

Reference

GRCh38 38.1/142

Chromosome

10

Position

103086421

Gene

CNNM2

is a	snp
is	mentioned by
dbSNP	rs11191548
dbSNP (classic)	rs11191548
ClinGen	rs11191548
ebi	rs11191548
HLI	rs11191548
Exac	rs11191548
Gnomad	rs11191548
Varsome	rs11191548
LitVar	rs11191548
Map	rs11191548
PheGenI	rs11191548
Biobank	rs11191548
1000 genomes	rs11191548
hgdp	rs11191548
ensembl	rs11191548
geneview	rs11191548
scholar	rs11191548
google	rs11191548
pharmgkb	rs11191548
gwascentral	rs11191548
openSNP	rs11191548
23andMe	rs11191548
SNPshot	rs11191548
SNPdbe	rs11191548
MSV3d	rs11191548
GWAS Ctlg	rs11191548

GMAF

0.1345

Max Magnitude

0

?

(C;C) (C;T) (T;T)

28

[PMID 19430483 ] 23andMe blog blood pressure

GWAS snp
PMID	[PMID 19430483 ]
Trait	Systolic blood pressure
Title	Genome-wide association study identifies eight loci associated with blood pressure
Risk Allele	T
P-val	7E-24
Odds Ratio	1.16 [0.92-1.40] mm Hg increase

GWAS snp
PMID	[PMID 21572416 ]
Trait
Title	Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians.
Risk Allele	T
P-val	4E-17
Odds Ratio	1.1800 [0.91-1.45] mm Hg increase

[PMID 21963141] Genetic variations in CYP17A1, CACNB2 and PLEKHA7 are associated with blood pressure and/or hypertension in she ethnic minority of China

GWAS snp
PMID	[PMID 21909115 ]
Trait
Title	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
Risk Allele	T
P-val	7E-26
Odds Ratio	1.0950 [NR] mmHg increase

GWAS snp
PMID	[PMID 21909110 ]
Trait
Title	Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.
Risk Allele	T
P-val	8E-11
Odds Ratio	0.5290 [0.37-0.69] mmHg increase

[PMID 20852445] Common variants in or near FGF5, CYP17A1 and MTHFR genes are associated with blood pressure and hypertension in Chinese Hans.

[PMID 22504314 ] Orthostatic hypotension and novel blood pressure-associated gene variants: Genetics of Postural Hemodynamics (GPH) Consortium.

[PMID 22525200] Pharmacogenetic implications for eight common blood pressure-associated single-nucleotide polymorphisms.

[PMID 23133444 ] Genetic variation in CYP17A1 is associated with arterial stiffness in diabetic subjects

[PMID 22048715] A sex-specific effect of the CYP17A1 SNP rs11191548 on blood pressure in Chinese children

[PMID 22959498] Recapitulation of four hypertension susceptibility genes (CSK, CYP17A1, MTHFR, and FGF5) in East Asians.

[PMID 23467202] Common polymorphism rs11191548 near the CYP17A1 gene is associated with hypertension and systolic blood pressure in the Han Chinese population.

[PMID 25917616] CYP17A1 and CYP2E1 Variants Associated with High Altitude Polycythemia in Tibetans at the Qinghai-Tibetan Plateau

[PMID 26263970 ] A Single Nucleotide Polymorphism near the CYP17A1 Gene Is Associated with Left Ventricular Mass in Hypertensive Patients under Pharmacotherapy