Human SNP ID | rs6591182 |
---|---|
Human chromosome | chr11 |
Human SNP position | 65582285 |
Pig chromosome | chr2 |
Pig SNP position | 5871107 |
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 (lobular) |
Initial sample | 236 European ancestry cases |
Replication sample | NA |
Region | 11q13.1 |
Chromosome id | chr11 |
Chromosome position | 65582285 |
Reported gene | LTBP3, EHBP1L1 |
Mapped gene | EHBP1L1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 254102 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs6591182-A |
SNPs | rs6591182 |
Merged | 0 |
SNP id current | 6591182 |
Context | missense_variant |
Intergenic | 0 |
Allele frequency | 0.47 |
P value | 0.0000009 |
Pvalue mlog | 6.04575749056067 |
P value text | |
Or beta | 0.54 |
%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 | GCST000766 |