Single nucleotide variant rs10030262
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.
There are no significant eQTL association in transcript level related to this SNP.
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| Marker ID | p-value | Regression coefficient | markerQTL plot | More |
|---|---|---|---|---|
| AMPA receptor ligand specific CNQX binding by autoradiography@hippocampus (subiculum) | 0.000000000781827 | 5.26641 | Display markerQTL plot |
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