Human SNP ID | rs2489715 |
---|---|
Human chromosome | chr10 |
Human SNP position | 42422028 |
Pig chromosome | chr15 |
Pig SNP position | 122443743 |
PubMed ID | 26105758 |
---|---|
Journal | Nat Commun |
Link | www.ncbi.nlm.nih.gov/pubmed/26105758 |
Study | A genome-wide association study identifies multiple loci for variation in human ear morphology. |
Disease/Trait | Helix rolling |
Initial sample | 4,919 Latin American individuals |
Replication sample | NA |
Region | 10q11.21 |
Chromosome id | chr10 |
Chromosome position | 42422028 |
Reported gene | NR |
Mapped gene | CCNYL2 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 414194 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs2489715-? |
SNPs | rs2489715 |
Merged | |
SNP id current | 2489715 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.0000008 |
Pvalue mlog | 6.09691001300805 |
P value text | (FDR adjusted) |
Or beta | |
%95 Ci | |
Platform | Illumina [671038] |
CNV | N |
Mapped trait | helix rolling |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0007670 |
Study accession | GCST002997 |