elevated systolic blood pressure Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Abnormal increase in systolic blood pressure. (Human Phenotype Ontology, HP_0004421)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0004421
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Genes

12 genes associated with the elevated systolic blood pressure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
ABCB11 ATP-binding cassette, sub-family B (MDR/TAP), member 11 0.942765
CLEC12B C-type lectin domain family 12, member B 0.919744
THRB thyroid hormone receptor, beta 0.882984
PLEKHG1 pleckstrin homology domain containing, family G (with RhoGef domain) member 1 0.868241
CSMD1 CUB and Sushi multiple domains 1 0.868241
SRGAP1 SLIT-ROBO Rho GTPase activating protein 1 0.848109
DSCAM Down syndrome cell adhesion molecule 0.836232
TMEM233 transmembrane protein 233 0.828053
CNTN4 contactin 4 0.799025
SNX29 sorting nexin 29 0.787244
DRD2 dopamine receptor D2 0.776638
CDH13 cadherin 13 0.773909