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SNP Report
Name | rs3789327 dbSNP Ensembl | ||
---|---|---|---|
Location | chr11:13363769 - 13363769(1) | ||
Variant Alleles | A/G | ||
Ancestral Allele | A | ||
Minor Allele | A | ||
Minor Allele Frequence | 0.458666 | ||
Functional Annotation | downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000529388); intron_variant(ENST00000389707, ENST00000401424, ENST00000403290, ENST00000403482, ENST00000403510, ENST00000497429, ENST00000530357); non_coding_transcript_variant(ENST00000497429); upstream_gene_variant(ENST00000534102) | ||
No. of Studies | 3 (Positive: 2; Negative: 1; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | YES |
Reference | Statistical Result | Description | Result Category |
---|---|---|---|
Soria, V.,2010 | X2-tests:allele P-value > 0.05, genotype P-value > 0.05 in all model | No significant association was observed. | Negative |