Human SNP ID | rs2295912 |
---|---|
Human chromosome | chrX |
Human SNP position | 108170700 |
Pig chromosome | chrX |
Pig SNP position | 103086839 |
PubMed ID | 25387706 |
---|---|
Journal | Psychophysiology |
Link | www.ncbi.nlm.nih.gov/pubmed/25387706 |
Study | Heritability and molecular genetic basis of electrodermal activity: A genome-wide association study. |
Disease/Trait | Electrodermal activity |
Initial sample | Up to 4,424 European ancestry twins and their parents |
Replication sample | NA |
Region | Xq22.3 |
Chromosome id | chrX |
Chromosome position | 108170700 |
Reported gene | COL4A6 |
Mapped gene | COL4A6 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 1288 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs2295912-? |
SNPs | rs2295912 |
Merged | 0 |
SNP id current | 2295912 |
Context | synonymous_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000002 |
Pvalue mlog | 5.69897000433601 |
P value text | (SCR Amplitude) |
Or beta | 0.058 |
%95 Ci | [0.034-0.082] unit increase |
Platform | Illumina [527829] |
CNV | N |
Mapped trait | electrodermal activity measurement, skin conductance response amplitude |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0006866, http://www.ebi.ac.uk/efo/EFO_0006868 |
Study accession | GCST002706 |