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- Data Summary
SNP Report
Basic Info
| Name | rs9011 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr5:112212608(Fwd) | ||
| Variant Alleles | G/T/A | ||
| Ancestral Allele | A | ||
| Functional Annotation | 3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant. | ||
| Consequence to Transcript | 3_prime_UTR_variant(ENST00000379638) NMD_transcript_variant(ENST00000506997) downstream_gene_variant(ENST00000513339; ENST00000261482; ENST00000497856; ENST00000511865; ENST00000545426) intron_variant(ENST00000509024; ENST00000503445; ENST00000512790; ENST00000506997) nc_transcript_variant(ENST00000509024; ENST00000503445; ENST00000512790) |
||
| 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: 1)
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.