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- Data Summary
SNP Report
Basic Info
| Name | rs2425046 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr20:33871661(Fwd) | ||
| Variant Alleles | T/C | ||
| Ancestral Allele | T | ||
| Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
| Consequence to Transcript | NMD_transcript_variant(ENST00000415116; ENST00000447927; ENST00000440766) downstream_gene_variant(ENST00000374408) intron_variant(ENST00000415116; ENST00000374443; ENST00000456600; ENST00000374436; ENST00000462894; ENST00000447927; ENST00000374450; ENST00000440766) nc_transcript_variant(ENST00000462894) upstream_gene_variant(ENST00000429167; ENST00000444717) |
||
| No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
| Source | LD-proxy | ||
SNP related studies (count: 0)
SNP related genes (count: 4)
Literature-origin genes (count: 0)
Genes from other sources 
(count: 4)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.