Human SNP ID | rs10776934 |
---|---|
Human chromosome | chr9 |
Human SNP position | 135137855 |
Pig chromosome | chr1 |
Pig SNP position | 308369136 |
PubMed ID | 22095909 |
---|---|
Journal | Hepatology |
Link | www.ncbi.nlm.nih.gov/pubmed/22095909 |
Study | Serum ferritin levels are associated with a distinct phenotype of chronic hepatitis C poorly responding to pegylated interferon-alpha and ribavirin therapy. |
Disease/Trait | Response to hepatitis C treatment |
Initial sample | 707 European ancestry cases |
Replication sample | NA |
Region | 9q34.3 |
Chromosome id | chr9 |
Chromosome position | 135137855 |
Reported gene | OLFM1 |
Mapped gene | OLFM1 - LOC102723948 |
Upstream gene id | 10439 |
Downstream gene id | 102723948 |
SNP gene ids | |
Upstream gene distance | 16671 |
Downstream gene distance | 24606 |
SNP risk allele | rs10776934-T |
SNPs | rs10776934 |
Merged | 0 |
SNP id current | 10776934 |
Context | regulatory_region_variant |
Intergenic | 1 |
Allele frequency | NR |
P value | 0.000001 |
Pvalue mlog | 6 |
P value text | |
Or beta | 0.281 |
%95 Ci | [0.17-0.39] ug/L decrease |
Platform | NR [NR] |
CNV | N |
Mapped trait | Chronic Hepatitis C infection |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004220 |
Study accession | GCST001325 |