Human SNP ID | rs932764 |
---|---|
Human chromosome | chr10 |
Human SNP position | 94136183 |
Pig chromosome | chr14 |
Pig SNP position | 115428971 |
PubMed ID | 21909115 |
---|---|
Journal | Nature |
Link | www.ncbi.nlm.nih.gov/pubmed/21909115 |
Study | Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. |
Disease/Trait | Systolic blood pressure |
Initial sample | 69,395 European ancestry individuals |
Replication sample | Up to 133,361 European ancestry individuals |
Region | 10q23.33 |
Chromosome id | chr10 |
Chromosome position | 94136183 |
Reported gene | PLCE1 |
Mapped gene | PLCE1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 51196 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs932764-G |
SNPs | rs932764 |
Merged | 0 |
SNP id current | 932764 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.44 |
P value | 0.0000000000000007 |
Pvalue mlog | 15.1549019599857 |
P value text | |
Or beta | 0.484 |
%95 Ci | [NR] mmHg increase |
Platform | Affymetrix, Illumina [~ 2500000] (imputed) |
CNV | N |
Mapped trait | systolic blood pressure |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0006335 |
Study accession | GCST001227 |
PubMed ID | 21909115 |
Journal | Nature |
Link | www.ncbi.nlm.nih.gov/pubmed/21909115 |
Study | Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. |
Disease/Trait | Diastolic blood pressure |
Initial sample | 69,395 European ancestry individuals |
Replication sample | Up to 133,361 European ancestry individuals |
Region | 10q23.33 |
Chromosome id | chr10 |
Chromosome position | 94136183 |
Reported gene | PLCE1 |
Mapped gene | PLCE1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 51196 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs932764-G |
SNPs | rs932764 |
Merged | 0 |
SNP id current | 932764 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.44 |
P value | 0.0000008 |
Pvalue mlog | 6.09691001300805 |
P value text | |
Or beta | 0.185 |
%95 Ci | [NR] mmHg increase |
Platform | Affymetrix, Illumina [~ 2500000] (imputed) |
CNV | N |
Mapped trait | diastolic blood pressure |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0006336 |
Study accession | GCST001228 |
PubMed ID | 21909115 |
Journal | Nature |
Link | www.ncbi.nlm.nih.gov/pubmed/21909115 |
Study | Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. |
Disease/Trait | Hypertension |
Initial sample | 69,395 European ancestry individuals |
Replication sample | Up to 133,361 European ancestry individuals |
Region | 10q23.33 |
Chromosome id | chr10 |
Chromosome position | 94136183 |
Reported gene | PLCE1 |
Mapped gene | PLCE1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 51196 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs932764-G |
SNPs | rs932764 |
Merged | 0 |
SNP id current | 932764 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.44 |
P value | 0.000000009 |
Pvalue mlog | 8.04575749056067 |
P value text | |
Or beta | 0.055 |
%95 Ci | [NR] unit increase |
Platform | Affymetrix, Illumina [~ 2500000] (imputed) |
CNV | N |
Mapped trait | hypertension |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0000537 |
Study accession | GCST001238 |