Human SNP ID | rs4730775 |
---|---|
Human chromosome | chr7 |
Human SNP position | 117277064 |
Pig chromosome | chr18 |
Pig SNP position | 30793432 |
PubMed ID | 21732829 |
---|---|
Journal | N Engl J Med |
Link | www.ncbi.nlm.nih.gov/pubmed/21732829 |
Study | Wnt signaling and Dupuytren__s disease. |
Disease/Trait | Dupuytren__s disease |
Initial sample | 856 European ancestry cases, 2,836 European ancestry controls |
Replication sample | 1,298 European ancestry cases, 7,136 European ancestry controls |
Region | 7q31.2 |
Chromosome id | chr7 |
Chromosome position | 117277064 |
Reported gene | WNT2 |
Mapped gene | WNT2 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 7472 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs4730775-? |
SNPs | rs4730775 |
Merged | 0 |
SNP id current | 4730775 |
Context | 3_prime_UTR_variant |
Intergenic | 0 |
Allele frequency | 0.59 |
P value | 0.00000003 |
Pvalue mlog | 7.52287874528033 |
P value text | |
Or beta | 1.2 |
%95 Ci | [1.14-1.30] |
Platform | Illumina [234939] |
CNV | N |
Mapped trait | Dupuytren Contracture |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004229 |
Study accession | GCST001144 |