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- Data Summary
SNP Report
Basic Info
| Name | rs3106191 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr6:33280505(Fwd) | ||
| Variant Alleles | C/A | ||
| Ancestral Allele | C | ||
| Functional Annotation | downstream_gene_variant; intron_variant; nc_transcript_variant. | ||
| Consequence to Transcript | downstream_gene_variant(ENST00000476333; ENST00000418724; ENST00000431845; ENST00000441117) intron_variant(ENST00000467025; ENST00000437116; ENST00000434618; ENST00000480730; ENST00000475304; ENST00000489157; ENST00000426633; ENST00000456592; LRG_114_t1) nc_transcript_variant(ENST00000437116; ENST00000480730) |
||
| 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.