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- Data Summary
SNP Report
Basic Info
| Name | rs690367 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr15:43748304(Fwd) | ||
| Variant Alleles | A/G | ||
| Ancestral Allele | G | ||
| Functional Annotation | NMD_transcript_variant; nc_transcript_variant; non_coding_exon_variant; synonymous_variant; upstream_gene_variant. | ||
| Consequence to Transcript | NMD_transcript_variant(ENST00000411772) nc_transcript_variant(ENST00000572085; ENST00000480860) non_coding_exon_variant(ENST00000572085; ENST00000480860) synonymous_variant(ENST00000263801; ENST00000411772; ENST00000450115; ENST00000413546; ENST00000382039; ENST00000382044) upstream_gene_variant(ENST00000414758) |
||
| No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
| Source | LD-proxy | ||
SNP related studies (count: 0)
SNP related genes (count: 1)
Literature-origin genes (count: 0)
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.