Human SNP ID | rs1378770 |
---|---|
Human chromosome | chr7 |
Human SNP position | 114723511 |
Pig chromosome | chr18 |
Pig SNP position | 33639494 |
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 | 7q31.1 |
Chromosome id | chr7 |
Chromosome position | 114723511 |
Reported gene | FOXP2 |
Mapped gene | FOXP2 - MDFIC |
Upstream gene id | 93986 |
Downstream gene id | 29969 |
SNP gene ids | |
Upstream gene distance | 29739 |
Downstream gene distance | 198643 |
SNP risk allele | rs1378770-G |
SNPs | rs1378770 |
Merged | 0 |
SNP id current | 1378770 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.15 |
P value | 0.000002 |
Pvalue mlog | 5.69897000433601 |
P value text | |
Or beta | 1.8 |
%95 Ci | |
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 |