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- Data Summary
SNP Report
Basic Info
| Name | rs790937 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr13:50651956(Fwd) | ||
| Variant Alleles | T/C | ||
| Ancestral Allele | T | ||
| Functional Annotation | intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000235290; ENST00000443587; ENST00000458725; ENST00000438752; ENST00000421758; ENST00000425586; ENST00000433070; ENST00000416253; ENST00000449579) nc_transcript_variant(ENST00000443587; ENST00000235290; ENST00000458725; ENST00000438752; ENST00000421758; ENST00000425586; ENST00000433070; ENST00000416253; ENST00000449579) upstream_gene_variant(ENST00000469754; ENST00000486895; ENST00000463474; ENST00000461527; ENST00000378180; ENST00000478860; ENST00000476738; ENST00000468168; ENST00000491341; ENST00000468522; ENST00000490577; ENST00000467721; ENST00000491615) |
||
| 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.