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- Data Summary
SNP Report
Basic Info
| Name | rs2260160 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr15:43895643(Fwd) | ||
| Variant Alleles | C/G/T/A | ||
| Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant. | ||
| Consequence to Transcript | NMD_transcript_variant(ENST00000428650; ENST00000440125) downstream_gene_variant(ENST00000300283; ENST00000410466; ENST00000455136; ENST00000441322; ENST00000437534) intron_variant(ENST00000411560; ENST00000450892; ENST00000485556; ENST00000428650; ENST00000541030; ENST00000396923; ENST00000471703; ENST00000440125; ENST00000448437) nc_transcript_variant(ENST00000493750; ENST00000411560; ENST00000485556; ENST00000471703; ENST00000448437) non_coding_exon_variant(ENST00000493750) upstream_gene_variant(ENST00000460952) |
||
| 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.