Human SNP ID | rs10129666 |
---|---|
Human chromosome | chr14 |
Human SNP position | 78228725 |
Pig chromosome | chr7 |
Pig SNP position | 107214210 |
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 | 14q24.3 |
Chromosome id | chr14 |
Chromosome position | 78228725 |
Reported gene | NRXN3 |
Mapped gene | NRXN3 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 9369 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs10129666-? |
SNPs | rs10129666 |
Merged | 0 |
SNP id current | 10129666 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000008 |
Pvalue mlog | 5.09691001300805 |
P value text | (SCR Amplitude) |
Or beta | 0.021 |
%95 Ci | [0.011-0.031] 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 |