Single nucleotide variant rs1003872
Genomic position: 4:
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
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| Transcript ID | Discovered on | cis/trans | Distance | p-value | Regression coefficient | eQTL plot | More |
|---|---|---|---|---|---|---|---|
| ENST00000475218 | Cerebellum | trans-eQTL | Distance not available. | 0.0000000179943 | 0.659533 | Display eQTL plot |
|
This SNP has no significant association with any pathology marker.