Human SNP ID | rs4844614 |
---|---|
Human chromosome | chr1 |
Human SNP position | 207701830 |
Pig chromosome | chr9 |
Pig SNP position | 74531535 |
PubMed ID | 19060910 |
---|---|
Journal | Nat Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/19060910 |
Study | Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. |
Disease/Trait | LDL cholesterol |
Initial sample | 4,763 Northern Finnish founder individuals |
Replication sample | NA |
Region | 1q32.2 |
Chromosome id | chr1 |
Chromosome position | 207701830 |
Reported gene | CR1L |
Mapped gene | CR1L |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 1379 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs4844614-A |
SNPs | rs4844614 |
Merged | 0 |
SNP id current | 4844614 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.32 |
P value | 0.0000002 |
Pvalue mlog | 6.69897000433601 |
P value text | |
Or beta | 0.1 |
%95 Ci | [0.06-0.14] mmol/l increase |
Platform | Illumina [329091] |
CNV | N |
Mapped trait | low density lipoprotein cholesterol measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004611 |
Study accession | GCST000283 |