Human SNP ID | rs9270986 |
---|---|
Human chromosome | chr6 |
Human SNP position | 32606283 |
Pig chromosome | chr7 |
Pig SNP position | 29139424 |
PubMed ID | 25643325 |
---|---|
Journal | JAMA Neurol |
Link | www.ncbi.nlm.nih.gov/pubmed/25643325 |
Study | A Genome-wide Association Study of Myasthenia Gravis. |
Disease/Trait | Myasthenia gravis |
Initial sample | 972 European ancestry cases, 1,977 European ancestry controls |
Replication sample | 423 European ancestry cases, 467 European ancestry controls |
Region | 6p21.32 |
Chromosome id | chr6 |
Chromosome position | 32606283 |
Reported gene | HLA-DRB1, HLA-DQA1 |
Mapped gene | HLA-DRB1 - HLA-DQA1 |
Upstream gene id | 3123 |
Downstream gene id | 3117 |
SNP gene ids | |
Upstream gene distance | 16447 |
Downstream gene distance | 31113 |
SNP risk allele | rs9270986-A |
SNPs | rs9270986 |
Merged | 0 |
SNP id current | 9270986 |
Context | intron_variant |
Intergenic | 1 |
Allele frequency | 0.15 |
P value | 0.00000006 |
Pvalue mlog | 7.22184874961635 |
P value text | |
Or beta | 1.43 |
%95 Ci | [NR] |
Platform | Illumina [8114394] (imputed) |
CNV | N |
Mapped trait | Myasthenia gravis |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004991 |
Study accession | GCST002838 |