Human SNP ID | rs3103778 |
---|---|
Human chromosome | chr1 |
Human SNP position | 39968099 |
Pig chromosome | chr6 |
Pig SNP position | 88943057 |
PubMed ID | 23534349 |
---|---|
Journal | Ann Hum Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/23534349 |
Study | Generalization of variants identified by genome-wide association studies for electrocardiographic traits in African Americans. |
Disease/Trait | PR interval |
Initial sample | 455 African American individuals |
Replication sample | NA |
Region | 1p34.2 |
Chromosome id | chr1 |
Chromosome position | 39968099 |
Reported gene | MFSD2 |
Mapped gene | MFSD2A |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 84879 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs3103778-G |
SNPs | rs3103778 |
Merged | 0 |
SNP id current | 3103778 |
Context | non_coding_transcript_exon_variant |
Intergenic | 0 |
Allele frequency | |
P value | 0.000009 |
Pvalue mlog | 5.04575749056067 |
P value text | |
Or beta | 6.3 |
%95 Ci | [NR] ms increase |
Platform | Illumina [> 930000] |
CNV | N |
Mapped trait | PR interval |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004462 |
Study accession | GCST001925 |