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SNP Report
Name | rs11022778 dbSNP Ensembl | ||
---|---|---|---|
Location | chr11:13369313 - 13369313(1) | ||
Variant Alleles | T/G | ||
Ancestral Allele | T | ||
Minor Allele | G | ||
Minor Allele Frequence | 0.276158 | ||
Functional Annotation | downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000530357); intron_variant(ENST00000389707, ENST00000401424, ENST00000403290, ENST00000403482, ENST00000403510, ENST00000497429, ENST00000534102); non_coding_transcript_variant(ENST00000497429, ENST00000534102); upstream_gene_variant(ENST00000524392, ENST00000529390) | ||
No. of Studies | 1 (Positive: 0; 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 = 0.125, Model Recessive, genotype P-value = 0.022, OR(95%CI)=1.67 (1.08-2.58) | Significant association was found. | Positive |