SNP Report
Basic Info
| Name | rs4963411 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 11:63412979 - 63412979(+) | ||
| Variant Seq | G | ||
| Ancestral Allele | C | ||
| Ref Seq | C | ||
| Minor Allele Frequence | 0.466054 | ||
| Annotation | downstream_gene_variant | ||
| Variant Effect | downstream_gene_variant(ENST00000536333, ENST00000279178) | ||
| SIFT Annotation | tolerated | ||
| SIFT Variant Effect | tolerated(ENST00000279178) | ||
| PolyPhen Annotation | benign | ||
| PolyPhen Variant Effect | benign(ENST00000279178) | ||
| 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)  |
|---|---|---|---|
| SLC22A9 | solute carrier family 22 (organic anion transporter), member 9 | 11q12.3 | Mapped by Literature SNP, Mapped by LD-proxy |
SNPs in LD with rs4963411 (count: 0)
SNP related eQTL (count: 1)