Human SNP ID | rs1529093 |
---|---|
Human chromosome | chr2 |
Human SNP position | 177044867 |
Pig chromosome | chr15 |
Pig SNP position | 92261150 |
PubMed ID | 20708005 |
---|---|
Journal | Gastroenterology |
Link | www.ncbi.nlm.nih.gov/pubmed/20708005 |
Study | Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. |
Disease/Trait | Non-alcoholic fatty liver disease histology (other) |
Initial sample | 236 European ancestry cases |
Replication sample | NA |
Region | 2q31.1 |
Chromosome id | chr2 |
Chromosome position | 177044867 |
Reported gene | intergenic |
Mapped gene | LOC105373761 - LOC105373760 |
Upstream gene id | 105373761 |
Downstream gene id | 105373760 |
SNP gene ids | |
Upstream gene distance | 9845 |
Downstream gene distance | 19452 |
SNP risk allele | rs1529093-A |
SNPs | rs1529093 |
Merged | 0 |
SNP id current | 1529093 |
Context | intron_variant |
Intergenic | 1 |
Allele frequency | 0.41 |
P value | 0.000002 |
Pvalue mlog | 5.69897000433601 |
P value text | (BallonTT) |
Or beta | 4.13 |
%95 Ci | [NR] unit increase |
Platform | Illumina [324623] |
CNV | N |
Mapped trait | non-alcoholic fatty liver disease, cirrhosis of liver |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0003095, http://www.ebi.ac.uk/efo/EFO_0001422 |
Study accession | GCST000765 |