Human SNP ID | rs10488172 |
---|---|
Human chromosome | chr7 |
Human SNP position | 133650423 |
Pig chromosome | chr18 |
Pig SNP position | 16530702 |
PubMed ID | 17903302 |
---|---|
Journal | BMC Med Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/17903302 |
Study | Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. |
Disease/Trait | Tonometry |
Initial sample | 644 individuals |
Replication sample | NA |
Region | 7q33 |
Chromosome id | chr7 |
Chromosome position | 133650423 |
Reported gene | EXOC4 |
Mapped gene | EXOC4 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 60412 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs10488172-? |
SNPs | rs10488172 |
Merged | 0 |
SNP id current | 10488172 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000008 |
Pvalue mlog | 5.09691001300805 |
P value text | (RWLTA) |
Or beta | |
%95 Ci | |
Platform | Affymetrix [70897] |
CNV | N |
Mapped trait | blood pressure |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004325 |
Study accession | GCST000107 |