SNP Report
Basic Info
| Name | rs5000695 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 8:130782089 - 130782089(+) | ||
| Variant Seq | T | ||
| Ancestral Allele | T | ||
| Ref Seq | C | ||
| Minor Allele Frequence | 0.483427 | ||
| Annotation | intron_variant | ||
| Variant Effect | intron_variant(ENST00000377928, ENST00000286355) | ||
| SIFT Annotation | tolerated | ||
| SIFT Variant Effect | tolerated(ENST00000286355, ENST00000377928) | ||
| PolyPhen Annotation | benign | ||
| PolyPhen Variant Effect | benign(ENST00000286355, ENST00000377928) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | n/a | ||
| Chromatin State | Weak transcription | ||
| No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||
SNP related association results
SNP related genes (count: 1)
| Approved Symbol | Approved Name | Location | No. of Association Results (Positive/Negative/Trend)  |
|---|---|---|---|
| ADCY8 | adenylate cyclase 8 (brain) | 8q24 | 1(0/0/1) |
SNPs in LD with rs5000695 (count: 0)
SNP related eQTL (count: 1)