Human SNP ID | rs117126031 |
---|---|
Human chromosome | chr20 |
Human SNP position | 49442326 |
Pig chromosome | chr17 |
Pig SNP position | 57425926 |
PubMed ID | 25663218 |
---|---|
Journal | Circ Cardiovasc Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/25663218 |
Study | Multiethnic genome-wide association study of cerebral white matter hyperintensities on MRI. |
Disease/Trait | White matter hyperintensity burden |
Initial sample | 17,936 European ancestry individuals, 1,943 African American ancestry individuals, 795 Hispanic individuals, 204 Chinese ancestry individuals, 201 Malay ancestry individuals |
Replication sample | NA |
Region | 20q13.13 |
Chromosome id | chr20 |
Chromosome position | 49442326 |
Reported gene | KCNB1 |
Mapped gene | KCNB1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 3745 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs117126031-A |
SNPs | rs117126031 |
Merged | |
SNP id current | 117126031 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.02 |
P value | 0.000006 |
Pvalue mlog | 5.22184874961635 |
P value text | |
Or beta | |
%95 Ci | |
Platform | Affymetrix, Illumina [14227402] (imputed) |
CNV | N |
Mapped trait | white matter hyperintensity measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0005665 |
Study accession | GCST003013 |
PubMed ID | 25663218 |
Journal | Circ Cardiovasc Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/25663218 |
Study | Multiethnic genome-wide association study of cerebral white matter hyperintensities on MRI. |
Disease/Trait | White matter hyperintensity burden |
Initial sample | 17,936 European ancestry individuals, 1,943 African American ancestry individuals, 795 Hispanic individuals, 204 Chinese ancestry individuals, 201 Malay ancestry individuals |
Replication sample | NA |
Region | 20q13.13 |
Chromosome id | chr20 |
Chromosome position | 49442326 |
Reported gene | KCNB1 |
Mapped gene | KCNB1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 3745 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs117126031-A |
SNPs | rs117126031 |
Merged | |
SNP id current | 117126031 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.02 |
P value | 0.000001 |
Pvalue mlog | 6 |
P value text | (EA) |
Or beta | |
%95 Ci | |
Platform | Affymetrix, Illumina [14227402] (imputed) |
CNV | N |
Mapped trait | white matter hyperintensity measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0005665 |
Study accession | GCST003013 |