Human SNP ID | rs11764932 |
---|---|
Human chromosome | chr7 |
Human SNP position | 15693493 |
Pig chromosome | chr9 |
Pig SNP position | 93669300 |
PubMed ID | 25493955 |
---|---|
Journal | Kidney Int |
Link | www.ncbi.nlm.nih.gov/pubmed/25493955 |
Study | Genome-wide association study of kidney function decline in individuals of European descent. |
Disease/Trait | Kidney function decline traits |
Initial sample | up to 45,530 European ancestry individuals |
Replication sample | up to 18,028 European ancestry individuals |
Region | 7p21.2 |
Chromosome id | chr7 |
Chromosome position | 15693493 |
Reported gene | MEOX2 |
Mapped gene | MEOX2-AS1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 101927524 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs11764932-A |
SNPs | rs11764932 |
Merged | 0 |
SNP id current | 11764932 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.36 |
P value | 0.0000004 |
Pvalue mlog | 6.39794000867203 |
P value text | (Rapid decline overall) |
Or beta | 0.09 |
%95 Ci | [NR] unit increase |
Platform | Affymetrix, Illumina [2500000] (imputed) |
CNV | N |
Mapped trait | rapid kidney function decline |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0006836 |
Study accession | GCST002720 |