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- Data Summary
SNP Report
Basic Info
| Name | rs2909786 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr5:112168065(Fwd) | ||
| Variant Alleles | A/G | ||
| Ancestral Allele | A | ||
| Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant. | ||
| Consequence to Transcript | NMD_transcript_variant(ENST00000508624; ENST00000520401) downstream_gene_variant(ENST00000505084) intron_variant(ENST00000508624; ENST00000507379; ENST00000257430; ENST00000457016; ENST00000520401; ENST00000508376; ENST00000502371; ENST00000504915; ENST00000512211; ENST00000514164; LRG_130_t1; LRG_130_t2; LRG_130_t3) nc_transcript_variant(ENST00000502371; ENST00000504915; ENST00000514164) |
||
| 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.