SNP Report
| Name | rs17763596 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 17:45843844 - 45843844(+) | ||
| Variant Seq | T | ||
| Ancestral Allele | G | ||
| Ref Seq | G | ||
| Minor Allele Frequence | 0.0860623 | ||
| Annotation | downstream_gene_variant; non_coding_transcript_exon_variant; upstream_gene_variant; non_coding_transcript_variant | ||
| Variant Effect | downstream_gene_variant(ENST00000581125, ENST00000579599); non_coding_transcript_exon_variant(ENST00000634876, ENST00000579244); upstream_gene_variant(ENST00000329196); non_coding_transcript_variant(ENST00000634876, ENST00000579244) | ||
| SIFT Annotation | tolerated | ||
| SIFT Variant Effect | tolerated(ENST00000329196) | ||
| PolyPhen Annotation | benign | ||
| PolyPhen Variant Effect | benign(ENST00000329196) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | TF binding region;lncRNA | ||
| Chromatin State | Weak transcription | ||
| No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||


