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- Data Summary
SNP Report
Basic Info
| Name | rs693510 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr15:43714625(Fwd) | ||
| Variant Alleles | C/G | ||
| Ancestral Allele | G | ||
| Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
| Consequence to Transcript | NMD_transcript_variant(ENST00000411772; ENST00000417342) intron_variant(ENST00000263801; ENST00000382044; ENST00000572085; ENST00000411772; ENST00000467474; ENST00000450115; ENST00000417342; ENST00000382039) nc_transcript_variant(ENST00000572085) upstream_gene_variant(ENST00000571145; ENST00000434561) |
||
| 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.