Human SNP ID | rs6991952 |
---|---|
Human chromosome | chr8 |
Human SNP position | 25849896 |
Pig chromosome | chr14 |
Pig SNP position | 10990141 |
PubMed ID | 26686553 |
---|---|
Journal | Nat Commun |
Link | www.ncbi.nlm.nih.gov/pubmed/26686553 |
Study | A genome-wide association study identifies four novel susceptibility loci underlying inguinal hernia. |
Disease/Trait | Inguinal hernia |
Initial sample | 5,295 European ancestry cases, 67,510 European ancestry controls |
Replication sample | 9,701 European ancestry cases, 82,743 European ancestry controls |
Region | 8p21.2 |
Chromosome id | chr8 |
Chromosome position | 25849896 |
Reported gene | EBF2 |
Mapped gene | LOC102723395, EBF2 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 102723395, 64641 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs6991952-G |
SNPs | rs6991952 |
Merged | |
SNP id current | 6991952 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.43 |
P value | 0.000000000000007 |
Pvalue mlog | 14.1549019599857 |
P value text | |
Or beta | 1.11 |
%95 Ci | [1.08-1.14] |
Platform | Affymetrix [6161781] (imputed) |
CNV | N |
Mapped trait | |
Mapped trait URI | |
Study accession | GCST003198 |