Human SNP ID | rs17067123 |
---|---|
Human chromosome | chr4 |
Human SNP position | 179127208 |
Pig chromosome | chr15 |
Pig SNP position | 47485223 |
PubMed ID | 19684573 |
---|---|
Journal | Nature |
Link | www.ncbi.nlm.nih.gov/pubmed/19684573 |
Study | Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance. |
Disease/Trait | Response to hepatitis C treatment |
Initial sample | 871 European ancestry cases, 191 African American cases, 75 Hispanic cases |
Replication sample | NA |
Region | 4q34.3 |
Chromosome id | chr4 |
Chromosome position | 179127208 |
Reported gene | intergenic |
Mapped gene | LOC105377563 - LOC105377564 |
Upstream gene id | 105377563 |
Downstream gene id | 105377564 |
SNP gene ids | |
Upstream gene distance | 309882 |
Downstream gene distance | 837651 |
SNP risk allele | rs17067123-? |
SNPs | rs17067123 |
Merged | 0 |
SNP id current | 17067123 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | NR |
P value | 0.000008 |
Pvalue mlog | 5.09691001300805 |
P value text | (combined) |
Or beta | |
%95 Ci | |
Platform | Illumina [565759] |
CNV | N |
Mapped trait | Chronic Hepatitis C infection |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004220 |
Study accession | GCST000465 |