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- Data Summary
SNP Report
Basic Info
| Name | rs4147730 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr11:47605427(Fwd) | ||
| Variant Alleles | G/A | ||
| Ancestral Allele | G | ||
| Functional Annotation | downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
| Consequence to Transcript | downstream_gene_variant(ENST00000524568; ENST00000530295; ENST00000528192; ENST00000533105; ENST00000529276; ENST00000531351; ENST00000534208; ENST00000534716) intron_variant(ENST00000263774; ENST00000526871; ENST00000533507; ENST00000525378; ENST00000525212; ENST00000527178) nc_transcript_variant(ENST00000526871; ENST00000525212; ENST00000525378; ENST00000533507; ENST00000527178) upstream_gene_variant(ENST00000526005; ENST00000530668; ENST00000356737; ENST00000529946; ENST00000538490; ENST00000395288; ENST00000430070; ENST00000529499; ENST00000534239) |
||
| No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
| Source | LD-proxy | ||
SNP related studies (count: 0)
SNP related genes (count: 4)
Literature-origin genes (count: 0)
Genes from other sources 
(count: 4)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.