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- Data Summary
SNP Report
Basic Info
| Name | rs12366302 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr12:102029166(Fwd) | ||
| Variant Alleles | C/T | ||
| Ancestral Allele | C | ||
| Functional Annotation | downstream_gene_variant; intron_variant; nc_transcript_variant. | ||
| Consequence to Transcript | downstream_gene_variant(ENST00000548834) intron_variant(ENST00000550514; ENST00000547509; ENST00000553190; ENST00000549145; ENST00000545503; ENST00000552198; ENST00000547405; ENST00000550501; ENST00000550312; ENST00000550270; ENST00000392934; ENST00000536007; ENST00000551300; ENST00000541119; ENST00000441232; ENST00000452455; ENST00000361466; ENST00000361685; ENST00000360610) nc_transcript_variant(ENST00000550312; ENST00000550501; ENST00000552198) |
||
| 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.