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- Data Summary
SNP Report
Basic Info
| Name | rs1709163 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr11:103278709(Fwd) | ||
| Variant Alleles | A/G | ||
| Ancestral Allele | G | ||
| 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(ENST00000528670) downstream_gene_variant(ENST00000528866) intron_variant(ENST00000334267; ENST00000375735; ENST00000528670; ENST00000398093; ENST00000533197) nc_transcript_variant(ENST00000522384) non_coding_exon_variant(ENST00000522384) upstream_gene_variant(ENST00000527233; ENST00000527650; ENST00000532655; ENST00000529569; ENST00000528255) |
||
| No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
| Source | LD-proxy | ||
SNP related studies (count: 0)
SNP related genes (count: 3)
Literature-origin genes (count: 0)
Genes from other sources 
(count: 3)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.