Rs11014166

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Orientationplus
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ReferenceGRCh37 37.1/131
Chromosome10
Position18708798
GeneCACNB2
is asnp
is mentioned by
dbSNPrs11014166
Exacrs11014166
PheGenIrs11014166
nextbiors11014166
hapmaprs11014166
1000 genomesrs11014166
hgdprs11014166
ensemblrs11014166
gopubmedrs11014166
geneviewrs11014166
scholarrs11014166
googlers11014166
pharmgkbrs11014166
gwascentralrs11014166
openSNPrs11014166
23andMers11014166
23andMe allrs11014166
SNP Nexus

SNPshotrs11014166
SNPdbers11014166
MSV3drs11014166
GMAF0.2034
? (A;A) (A;T) (T;T) 28
23andMe blog blood pressure
GWAS snp
PMID [PMID 19430479OA-icon.png]
Trait Diastolic Blood Pressure
Title Genome-wide association study of blood pressure and hypertension
Risk Allele A
P-val 1E-8
Odds Ratio 0.37 [0.25-0.49] mm Hg increase

[PMID 21156931OA-icon.png] Genetic Variation in the {beta}2 Subunit of the Voltage-Gated Calcium Channel and Pharmacogenetic Association With Adverse Cardiovascular Outcomes in the INternational VErapamil SR-Trandolapril STudy GENEtic Substudy (INVEST-GENES)


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

GET Evidence
rs11014166
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.3125
summary



[PMID 23744328] [Association between CACNB2 gene polymorphisms and essential hypertension]