Human SNP ID | rs1051920 |
---|---|
Human chromosome | chr8 |
Human SNP position | 80526185 |
Pig chromosome | chr4 |
Pig SNP position | 61307125 |
PubMed ID | 22493691 |
---|---|
Journal | PLoS One |
Link | www.ncbi.nlm.nih.gov/pubmed/22493691 |
Study | Novel associations for hypothyroidism include known autoimmune risk loci. |
Disease/Trait | Hypothyroidism |
Initial sample | 3,736 European ancestry cases, 35,546 European ancestry controls |
Replication sample | NA |
Region | 8q21.13 |
Chromosome id | chr8 |
Chromosome position | 80526185 |
Reported gene | ZBTB10, RPSAP47 |
Mapped gene | ZBTB10 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 65986 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs1051920-T |
SNPs | rs1051920 |
Merged | 0 |
SNP id current | 1051920 |
Context | 3_prime_UTR_variant |
Intergenic | 0 |
Allele frequency | 0.254 |
P value | 0.000004 |
Pvalue mlog | 5.39794000867203 |
P value text | |
Or beta | 1.143 |
%95 Ci | [1.08-1.21] |
Platform | Illumina [870065] |
CNV | N |
Mapped trait | hypothyroidism |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004705 |
Study accession | GCST001474 |