Human SNP ID | rs17767392 |
---|---|
Human chromosome | chr14 |
Human SNP position | 71298060 |
Pig chromosome | chr7 |
Pig SNP position | 101011799 |
PubMed ID | 26301497 |
---|---|
Journal | Nat Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/26301497 |
Study | Genetic association analyses highlight biological pathways underlying mitral valve prolapse. |
Disease/Trait | Mitral valve prolapse |
Initial sample | 1,442 European ancestry cases, 2,439 European ancestry controls |
Replication sample | 1,422 European ancestry cases, 6,779 European ancestry controls |
Region | 14q24.2 |
Chromosome id | chr14 |
Chromosome position | 71298060 |
Reported gene | PCNX, SIPA1L1 |
Mapped gene | LOC102724015 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 102724015 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs17767392-T |
SNPs | rs17767392 |
Merged | |
SNP id current | 17767392 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.25 |
P value | 0.00000002 |
Pvalue mlog | 7.69897000433601 |
P value text | |
Or beta | 1.23 |
%95 Ci | [1.15-1.32] |
Platform | Affymetrix, Illumina [~ 4800000] (imputed) |
CNV | N |
Mapped trait | Mitral valve prolapse |
Mapped trait URI | http://purl.obolibrary.org/obo/HP_0001634 |
Study accession | GCST003094 |