Human SNP ID | rs770189 |
---|---|
Human chromosome | chr5 |
Human SNP position | 88792622 |
Pig chromosome | chr2 |
Pig SNP position | 98861348 |
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 | 5q14.3 |
Chromosome id | chr5 |
Chromosome position | 88792622 |
Reported gene | MEF2C |
Mapped gene | MEF2C |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 4208 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs770189-? |
SNPs | rs770189 |
Merged | 0 |
SNP id current | 770189 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000003 |
Pvalue mlog | 5.52287874528033 |
P value text | (CB-PWV) |
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 |