SNP Report
Basic Info
| Name | rs62516744 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 8:42707819 - 42707819(+) | ||
| Variant Seq | G | ||
| Ancestral Allele | A | ||
| Ref Seq | A | ||
| Minor Allele Frequence | 0.0389377 | ||
| Annotation | intron_variant; non_coding_transcript_variant | ||
| Variant Effect | intron_variant(ENST00000534391, ENST00000527318, ENST00000289957, ENST00000531610); non_coding_transcript_variant(ENST00000527318, ENST00000531610) | ||
| SIFT Annotation | tolerated | ||
| SIFT Variant Effect | tolerated(ENST00000289957) | ||
| PolyPhen Annotation | benign | ||
| PolyPhen Variant Effect | benign(ENST00000289957) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | n/a | ||
| Chromatin State | Weak transcription;Enhancers | ||
| 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)  |
|---|---|---|---|
| CHRNB3 | cholinergic receptor, nicotinic beta 3 | 8p11.21 | Mapped by Literature SNP, Mapped by LD-proxy |
SNPs in LD with rs62516744 (count: 0)
SNP related eQTL (count: 1)