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SNP Report
Name | rs2640909 dbSNP Ensembl | ||
---|---|---|---|
Location | chr1:7830057 - 7830057(1) | ||
Variant Alleles | T/C | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.185304 | ||
Functional Annotation | missense_variant; upstream_gene_variant.
Polyphen Annotation: benign(ENST00000614998, ENST00000361923, ENST00000377532, ENST00000613533) SIFT Annotation: tolerated - low confidence(ENST00000361923, ENST00000377532, ENST00000613533); tolerated(ENST00000614998) |
||
Consequence to Transcript | missense_variant(ENST00000614998, ENST00000361923, ENST00000377532, ENST00000613533); upstream_gene_variant(ENST00000451646) | ||
No. of Studies | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | YES | ||
Overlap with MDD? | NO |
Reference | Statistical Result | Description | Result Category |
---|---|---|---|
Mansour, H. A.,2009 | Single SNP-based analyses:Trends test P-value = 0.031 in SZ | Significant association was observed | Positive |