SNP Report
Basic Info
| Name | rs6355 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 17:30221792 - 30221792(+) | ||
| Variant Seq | G | ||
| Ancestral Allele | C | ||
| Ref Seq | C | ||
| Minor Allele Frequence | 0.00698882 | ||
| Annotation | missense_variant | ||
| Variant Effect | missense_variant(ENST00000261707, ENST00000394821, ENST00000401766) | ||
| SIFT Annotation | tolerated | ||
| SIFT Variant Effect | tolerated(ENST00000261707, ENST00000394821, ENST00000401766) | ||
| PolyPhen Annotation | benign | ||
| PolyPhen Variant Effect | benign(ENST00000261707, ENST00000394821, ENST00000401766) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | n/a | ||
| Chromatin State | Weak transcription;Enhancers;Flanking Active TSS | ||
| 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)  |
|---|---|---|---|
| SLC6A4 | solute carrier family 6 (neurotransmitter transporter), member 4 | 17q11.2 | 44(13/31/0) |
SNPs in LD with rs6355 (count: 0)
SNP related eQTL (count: 1)