Single nucleotide variant rs9569035
Genomic position: 13:
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 |
|---|---|---|---|---|
| CRHR2 RNA by in situ hybridization@frontal (white matter/B5) | 0.0000000000259248 | 7.00001 | Display markerQTL plot |
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