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- Data Summary
SNP Report
Basic Info
| Name | rs12360820 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr11:620927(Fwd) | ||
| Variant Alleles | A/C | ||
| Ancestral Allele | A | ||
| Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
| Consequence to Transcript | NMD_transcript_variant(ENST00000531177) downstream_gene_variant(ENST00000531088; ENST00000526077; ENST00000534311; ENST00000529337) intron_variant(ENST00000358353; ENST00000349570; ENST00000531899; ENST00000397542; ENST00000532949; ENST00000531177) nc_transcript_variant(ENST00000531899; ENST00000532949) upstream_gene_variant(ENST00000533182; ENST00000397574; ENST00000532326; ENST00000532788; ENST00000397570; ENST00000533190; ENST00000397562; ENST00000330243) |
||
| No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
| Source | LD-proxy | ||
SNP related studies (count: 0)
SNP related genes (count: 2)
Literature-origin genes (count: 0)
Genes from other sources 
(count: 2)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.