SNP Report
Basic Info
| Name | rs4660346 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 1:46422367 - 46422367(+) | ||
| Variant Seq | C,T | ||
| Ancestral Allele | C | ||
| Ref Seq | A | ||
| Minor Allele Frequence | 0.333267 | ||
| Annotation | synonymous_variant; downstream_gene_variant; 3_prime_UTR_variant; NMD_transcript_variant | ||
| SIFT Annotation | deleterious | ||
| SIFT Variant Effect | deleterious(ENST00000243167) | ||
| PolyPhen Annotation | probably_damaging | ||
| PolyPhen Variant Effect | probably_damaging(ENST00000243167) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | n/a | ||
| Chromatin State | Weak transcription;Bivalent Enhancer;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: 0)
SNPs in LD with rs4660346 (count: 0)
SNP related eQTL (count: 1)