Search SNP
Search Gene
Search CNV
Search Haplotype
Search Other Variant
Search Region
Search Pathway
Search Study
SNP Report
| Name | rs956572 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr18:63153338 - 63153338(1) | ||
| Variant Alleles | A/G | ||
| Ancestral Allele | G | ||
| Minor Allele | A | ||
| Minor Allele Frequence | 0.349042 | ||
| Functional Annotation | intron_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000333681, ENST00000398117, ENST00000590515); non_coding_transcript_variant(ENST00000590515); upstream_gene_variant(ENST00000587475) | ||
| No. of Studies | 2 (Positive: 0; Negative: 2; Trend: 0) | ||
| Source | Literature | ||
| Overlap with SZ? | NO | ||
| Overlap with MDD? | YES | ||
| Reference | Statistical Result | Description | Result Category |
|---|---|---|---|
| Uemura, T.,2011 | chi-square tests:genotype, MDD(P-value = 0.31, X2=2.32);allele, MDD[P-value = 0.89;OR = 0.95, 95% CI:(0.52-1.75), X2=0.02] | No significant association was observed. | Negative |


