Human SNP ID | rs11067763 |
---|---|
Human chromosome | chr12 |
Human SNP position | 115760536 |
Pig chromosome | chr14 |
Pig SNP position | 38857800 |
PubMed ID | 25249183 |
---|---|
Journal | Hum Mol Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/25249183 |
Study | Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension. |
Disease/Trait | Systolic blood pressure |
Initial sample | 11,816 Han Chinese ancestry individuals |
Replication sample | 69,146 Han Chinese ancestry individuals |
Region | 12q24.21 |
Chromosome id | chr12 |
Chromosome position | 115760536 |
Reported gene | MED13L |
Mapped gene | LOC105370003 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 105370003 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs11067763-A |
SNPs | rs11067763 |
Merged | 0 |
SNP id current | 11067763 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.62 |
P value | 0.0000000000000006 |
Pvalue mlog | 15.2218487496163 |
P value text | |
Or beta | 0.81 |
%95 Ci | [0.61-1.01] unit increase |
Platform | Affymetrix, Illumina [2485448] (imputed) |
CNV | N |
Mapped trait | systolic blood pressure |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0006335 |
Study accession | GCST002630 |
PubMed ID | 25249183 |
Journal | Hum Mol Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/25249183 |
Study | Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension. |
Disease/Trait | Diastolic blood pressure |
Initial sample | 11,816 Han Chinese ancestry individuals |
Replication sample | 69,146 Han Chinese ancestry individuals |
Region | 12q24.21 |
Chromosome id | chr12 |
Chromosome position | 115760536 |
Reported gene | MED13L |
Mapped gene | LOC105370003 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 105370003 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs11067763-A |
SNPs | rs11067763 |
Merged | 0 |
SNP id current | 11067763 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.62 |
P value | 0.000000000000000002 |
Pvalue mlog | 17.698970004336 |
P value text | |
Or beta | 0.51 |
%95 Ci | [0.39-0.63] unit increase |
Platform | Affymetrix, Illumina [2485448] (imputed) |
CNV | N |
Mapped trait | diastolic blood pressure |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0006336 |
Study accession | GCST002631 |
PubMed ID | 25249183 |
Journal | Hum Mol Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/25249183 |
Study | Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension. |
Disease/Trait | Hypertension |
Initial sample | 5,065 Han Chinese ancestry cases, 4,404 Han Chinese ancestry controls |
Replication sample | 29,799 Han Chinese ancestry cases, 39,347 Han Chinese ancestry controls |
Region | 12q24.21 |
Chromosome id | chr12 |
Chromosome position | 115760536 |
Reported gene | MED13L |
Mapped gene | LOC105370003 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 105370003 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs11067763-A |
SNPs | rs11067763 |
Merged | 0 |
SNP id current | 11067763 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.62 |
P value | 0.0000001 |
Pvalue mlog | 7 |
P value text | |
Or beta | |
%95 Ci | |
Platform | Affymetrix, Illumina [2485448] (imputed) |
CNV | N |
Mapped trait | hypertension |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0000537 |
Study accession | GCST002627 |