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- Data Summary
SNP Report
Basic Info
| Name | rs9394145 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr6:33399778(Fwd) | ||
| Variant Alleles | C/T | ||
| Ancestral Allele | C | ||
| Functional Annotation | intron_variant; missense_variant; nc_transcript_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000449372; ENST00000479510; ENST00000496374; ENST00000418600; ENST00000293748) missense_variant(ENST00000428982) nc_transcript_variant(ENST00000479510; ENST00000496374) |
||
| 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.