Human SNP ID | rs1861960 |
---|---|
Human chromosome | chr7 |
Human SNP position | 155492440 |
Pig chromosome | chr18 |
Pig SNP position | 2966480 |
PubMed ID | 23793025 |
---|---|
Journal | Nat Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/23793025 |
Study | Genome-wide meta-analysis identifies new susceptibility loci for migraine. |
Disease/Trait | Migraine |
Initial sample | 23,285 European ancestry cases, 95,425 European ancestry controls |
Replication sample | NA |
Region | 7q36.3 |
Chromosome id | chr7 |
Chromosome position | 155492440 |
Reported gene | intergenic |
Mapped gene | EN2 - CNPY1 |
Upstream gene id | 2020 |
Downstream gene id | 285888 |
SNP gene ids | |
Upstream gene distance | 27609 |
Downstream gene distance | 8818 |
SNP risk allele | rs1861960-T |
SNPs | rs1861960 |
Merged | 0 |
SNP id current | 1861960 |
Context | intron_variant |
Intergenic | 1 |
Allele frequency | 0.2 |
P value | 0.000006 |
Pvalue mlog | 5.22184874961635 |
P value text | |
Or beta | 1.07 |
%95 Ci | [1.04-1.10] |
Platform | Affymetrix, Illumina [~ 2300000] (imputed) |
CNV | N |
Mapped trait | migraine disorder |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0003821 |
Study accession | GCST002081 |