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- Data Summary
SNP Report
Basic Info
| Name | rs936470 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr11:606656(Fwd) | ||
| Variant Alleles | G/C | ||
| Ancestral Allele | C | ||
| Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant. | ||
| Consequence to Transcript | NMD_transcript_variant(ENST00000534320) intron_variant(ENST00000534320; ENST00000413872; ENST00000526724; ENST00000416188; ENST00000533464; ENST00000264555) nc_transcript_variant(ENST00000532550; ENST00000526724) non_coding_exon_variant(ENST00000532550) upstream_gene_variant(ENST00000525848) |
||
| 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.