Single nucleotide variant rs10160281
Genomic position: 11:
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
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| Transcript ID | Discovered on | cis/trans | Distance | p-value | Regression coefficient | eQTL plot | More |
|---|---|---|---|---|---|---|---|
| ENST00000265909 | Prefrontal Cortex | cis-eQTL | 2543 | 0.0000000318422 | -0.899559 | Display eQTL plot |
|
This SNP has no significant association with any pathology marker.