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- Data Summary
SNP Report
Basic Info
| Name | rs6433953 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr2:182911702(Fwd) | ||
| Variant Alleles | C/T | ||
| Ancestral Allele | C | ||
| Functional Annotation | intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000486067; ENST00000495820; ENST00000464264; ENST00000475249; ENST00000409702; ENST00000490645; ENST00000280295; ENST00000465612; ENST00000479855; ENST00000409137; ENST00000452904) nc_transcript_variant(ENST00000475249; ENST00000495820; ENST00000464264; ENST00000486067; ENST00000465612; ENST00000479855; ENST00000490645) upstream_gene_variant(ENST00000410486) |
||
| 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.