Human SNP ID | rs205611 |
---|---|
Human chromosome | chr2 |
Human SNP position | 74744954 |
Pig chromosome | chr3 |
Pig SNP position | 71486496 |
PubMed ID | 21835309 |
---|---|
Journal | Am J Hum Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/21835309 |
Study | GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development. |
Disease/Trait | Iris characteristics |
Initial sample | 2,121 European ancestry individuals |
Replication sample | 499 European ancestry adolescent twins and siblings, 73 European ancestry adult individuals |
Region | 2p13.1 |
Chromosome id | chr2 |
Chromosome position | 74744954 |
Reported gene | AC007387.1 |
Mapped gene | LOC102724497 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 102724497 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs205611-A |
SNPs | rs205611 |
Merged | 0 |
SNP id current | 205611 |
Context | intergenic_variant |
Intergenic | 0 |
Allele frequency | |
P value | 0.000001 |
Pvalue mlog | 6 |
P value text | (Crypts) |
Or beta | 0.12 |
%95 Ci | [0.06-0.18] unit decrease |
Platform | Illumina [274604] (imputed) |
CNV | N |
Mapped trait | eye measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004731 |
Study accession | GCST001199 |