Single nucleotide variant rs2147897
Genomic position: 10:
Allele info and frequencies
This SNP has no significant association with diseases nor in high LD with index SNPs.
There are no significant eQTL association in gene level to this SNP.
Transcript Level
Click on transcript id to go to that transcript. Cilck table header to sort by that attribute.
| Transcript ID | Discovered on | cis/trans | Distance | p-value | Regression coefficient | eQTL plot | More |
|---|---|---|---|---|---|---|---|
| ENST00000370575 | Prefrontal Cortex | cis-eQTL | 0 | 0.0000000979202 | 0.992527 | Display eQTL plot |
|
Click on marker name to go to that marker. Cilck table header to sort by that attribute.
| Marker ID | p-value | Regression coefficient | markerQTL plot | More |
|---|---|---|---|---|
| N6-Methyllysine by mass spectrometry@hippocampus | 0.000000000944831 | -0.00842177 | Display markerQTL plot |
|
| N6-Methyllysine by mass spectrometry@frontal | 0.000000000146513 | -0.00741855 | Display markerQTL plot |
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