SNP Report

Basic Info
| Name |
rs9378249
dbSNP
Ensembl
|
| Location |
chrCHR_HSCHR6_MHC_SSTO_CTG1:31353627 - 31353627(1) |
| Variant Alleles |
T/G |
| Minor Allele |
G |
| Minor Allele Frequence |
0.0686901 |
| Functional Annotation |
downstream_gene_variant; upstream_gene_variant.
|
| Consequence to Transcript |
downstream_gene_variant(ENST00000603274); upstream_gene_variant(ENST00000412585, ENST00000434333, ENST00000463574, ENST00000474381, ENST00000497377, ENST00000498007, ENST00000618788, ENST00000416726, ENST00000425848, ENST00000445222, ENST00000461583, ENST00000470915, ENST00000473379, ENST00000490676, ENST00000430299, ENST00000435618, ENST00000436729, ENST00000465455, ENST00000481283, ENST00000488367, ENST00000489762, ENST00000425798, ENST00000437866, ENST00000450871, ENST00000462100, ENST00000469883, ENST00000471639, ENST00000494335, ENST00000359635, ENST00000418147, ENST00000466304, ENST00000475493, ENST00000479203, ENST00000479990, ENST00000493512, ENST00000421349, ENST00000437265, ENST00000445610, ENST00000463600, ENST00000463832, ENST00000475902, ENST00000498484) |
| No. of Studies |
2 (Positive: 1; Negative: 0; Trend: 1) |
| Source |
Literature |
| Overlap with SZ? |
NO
|
| Overlap with MDD? |
NO
|

SNP related studies (count: 2)

SNP related genes (count: 1)

Overlap with SZ from cross-disorder studies (count: 0)

Overlap with MDD from cross-disorder studies (count: 0)