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- Data Summary
SNP Report
Basic Info
| Name | rs211114 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr11:18001888(Fwd) | ||
| Variant Alleles | C/T | ||
| Ancestral Allele | C | ||
| Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant. | ||
| Consequence to Transcript | NMD_transcript_variant(ENST00000525422; ENST00000527494; ENST00000532546) intron_variant(ENST00000525422; ENST00000527494; ENST00000265965; ENST00000529440; ENST00000528200; ENST00000529151; ENST00000533241; ENST00000525920; ENST00000532265; ENST00000529728; ENST00000532546) nc_transcript_variant(ENST00000529440) |
||
| 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.