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- Data Summary
SNP Report
Basic Info
| Name | rs1176713 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr11:113860425(Fwd) | ||
| Variant Alleles | A/G | ||
| Ancestral Allele | G | ||
| Functional Annotation | 3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; synonymous_variant. | ||
| Consequence to Transcript | 3_prime_UTR_variant(ENST00000510849) NMD_transcript_variant(ENST00000510849) downstream_gene_variant(ENST00000502622) synonymous_variant(ENST00000504030; ENST00000535865; ENST00000375498; ENST00000355556; ENST00000299961; ENST00000506841) |
||
| 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: 1)
Genes from other sources 
(count: 0)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.