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- Data Summary
SNP Report
Basic Info
| Name | rs4846054 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr1:11869230(Fwd) | ||
| Variant Alleles | C/T | ||
| Ancestral Allele | C | ||
| Functional Annotation | intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000376497; ENST00000346436; ENST00000376496; ENST00000376491; ENST00000376490; ENST00000376487; ENST00000376492; ENST00000312413) nc_transcript_variant(ENST00000376491; ENST00000376490; ENST00000376492) upstream_gene_variant(ENST00000423400; ENST00000376486; ENST00000418034; ENST00000376585; ENST00000376590; ENST00000413656; ENST00000431243) |
||
| No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
| Source | LD-proxy | ||
SNP related studies (count: 0)
SNP related genes (count: 2)
Literature-origin genes (count: 1)
Genes from other sources 
(count: 1)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.