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SNP Report
Name | rs37022 dbSNP Ensembl | ||
---|---|---|---|
Location | chrCHR_HSCHR5_3_CTG1:1413658 - 1413658(-1) | ||
Variant Alleles | A/T | ||
Ancestral Allele | A | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.355631 | ||
Functional Annotation | intron_variant; non_coding_transcript_variant; downstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000270349, ENST00000511750); non_coding_transcript_variant(ENST00000511750); downstream_gene_variant(ENST00000626610, ENST00000621716) | ||
No. of Studies | 3 (Positive: 1; Negative: 2; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | YES | ||
Overlap with MDD? | NO |
Reference | Statistical Result | Description | Result Category |
---|---|---|---|
Pinsonneault, J. K.,2011 | Stanley sample:allele, X2 P-value = 0.81, Fisher's exact P-value = 0.86OR=0.91 for SZ | No significant association was observed. | Negative |