Human SNP ID | rs10501320 |
---|---|
Human chromosome | chr11 |
Human SNP position | 47272248 |
Pig chromosome | chr2 |
Pig SNP position | 16536506 |
PubMed ID | 21873549 |
---|---|
Journal | Diabetes |
Link | www.ncbi.nlm.nih.gov/pubmed/21873549 |
Study | Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes. |
Disease/Trait | Proinsulin levels |
Initial sample | 10,701 European ancestry individuals |
Replication sample | 16,378 European ancestry individuals |
Region | 11p11.2 |
Chromosome id | chr11 |
Chromosome position | 47272248 |
Reported gene | MADD |
Mapped gene | MADD |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 8567 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs10501320-G |
SNPs | rs10501320 |
Merged | 0 |
SNP id current | 10501320 |
Context | 5_prime_UTR_variant |
Intergenic | 0 |
Allele frequency | 0.72 |
P value | 1E-88 |
Pvalue mlog | 88 |
P value text | |
Or beta | |
%95 Ci | |
Platform | Affymetrix, Illumina [~ 2500000] (imputed) |
CNV | N |
Mapped trait | insulin measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004467 |
Study accession | GCST001212 |