Human SNP ID | rs727979 |
---|---|
Human chromosome | chr6 |
Human SNP position | 149272784 |
Pig chromosome | chr1 |
Pig SNP position | 18968175 |
PubMed ID | 17903294 |
---|---|
Journal | BMC Med Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/17903294 |
Study | Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. |
Disease/Trait | Hemostatic factors and hematological phenotypes |
Initial sample | Up to 1,062 European ancestry individuals |
Replication sample | NA |
Region | 6q25.1 |
Chromosome id | chr6 |
Chromosome position | 149272784 |
Reported gene | MAP3K7IP2 |
Mapped gene | TAB2 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 23118 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs727979-? |
SNPs | rs727979 |
Merged | 0 |
SNP id current | 727979 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.14 |
P value | 0.000008 |
Pvalue mlog | 5.09691001300805 |
P value text | (RBCC) |
Or beta | |
%95 Ci | |
Platform | Affymetrix [70897] |
CNV | N |
Mapped trait | erythrocyte count |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004305 |
Study accession | GCST000080 |