Human SNP ID | rs10831496 |
---|---|
Human chromosome | chr11 |
Human SNP position | 88824823 |
Pig chromosome | chr9 |
Pig SNP position | 24638663 |
PubMed ID | 19340012 |
---|---|
Journal | J Invest Dermatol |
Link | www.ncbi.nlm.nih.gov/pubmed/19340012 |
Study | Genome-wide association study of tanning phenotype in a population of European ancestry. |
Disease/Trait | Tanning |
Initial sample | 2,287 European ancestry female individuals |
Replication sample | 870 European ancestry female individuals |
Region | 11q14.3 |
Chromosome id | chr11 |
Chromosome position | 88824823 |
Reported gene | GRM5 |
Mapped gene | GRM5 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 2915 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs10831496-G |
SNPs | rs10831496 |
Merged | 0 |
SNP id current | 10831496 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000000005 |
Pvalue mlog | 8.30102999566398 |
P value text | |
Or beta | 0.14 |
%95 Ci | [0.10-0.18] tanning ability score decrease |
Platform | Illumina [528173] |
CNV | N |
Mapped trait | suntan |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004279 |
Study accession | GCST000371 |