Human SNP ID | rs1950626 |
---|---|
Human chromosome | chr14 |
Human SNP position | 100907636 |
Pig chromosome | chr7 |
Pig SNP position | 132067420 |
PubMed ID | 26545240 |
---|---|
Journal | PLoS One |
Link | www.ncbi.nlm.nih.gov/pubmed/26545240 |
Study | Genetic Determinants of Pelvic Organ Prolapse among African American and Hispanic Women in the Women__s Health Initiative. |
Disease/Trait | Pelvic organ prolapse (moderate/severe) |
Initial sample | 154 African American cases, 948 African American controls, 163 Hispanic cases, 305 Hispanic controls |
Replication sample | NA |
Region | 14q32.31 |
Chromosome id | chr14 |
Chromosome position | 100907636 |
Reported gene | AL132709.5, MIR370, RTL1 |
Mapped gene | MEG8 - MIR370 |
Upstream gene id | 79104 |
Downstream gene id | 442915 |
SNP gene ids | |
Upstream gene distance | 668 |
Downstream gene distance | 3503 |
SNP risk allele | rs1950626-G |
SNPs | rs1950626 |
Merged | 0 |
SNP id current | 1950626 |
Context | intron_variant |
Intergenic | 1 |
Allele frequency | 0.79 |
P value | 0.0000003 |
Pvalue mlog | 6.52287874528033 |
P value text | (Hispanic) |
Or beta | 2.96 |
%95 Ci | [1.96-4.48] |
Platform | Affymetrix [at least 730985] (imputed) |
CNV | N |
Mapped trait | pelvic organ prolapse |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004710 |
Study accession | GCST003225 |