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- Data Summary
SNP Report
Basic Info
| Name | rs1055075 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr11:113239512(Fwd) | ||
| Variant Alleles | T/C | ||
| Ancestral Allele | C | ||
| Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant. | ||
| Consequence to Transcript | NMD_transcript_variant(ENST00000462711; ENST00000494714; ENST00000575621; ENST00000572987) downstream_gene_variant(ENST00000529221; ENST00000480233; ENST00000483239; ENST00000496311; ENST00000464224; ENST00000314756; ENST00000575184; ENST00000576717; ENST00000574586; ENST00000572649; ENST00000570674) intron_variant(ENST00000393020; ENST00000462711; ENST00000494714; ENST00000575621; ENST00000572987; ENST00000574319) |
||
| 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.