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- Data Summary
SNP Report
Basic Info
| Name | rs8352 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr5:1463051(Fwd) | ||
| Variant Alleles | G/C | ||
| Ancestral Allele | G | ||
| Functional Annotation | 3_prime_UTR_variant; NMD_transcript_variant; nc_transcript_variant; non_coding_exon_variant. | ||
| Consequence to Transcript | 3_prime_UTR_variant(ENST00000475622; ENST00000283415) NMD_transcript_variant(ENST00000475622) nc_transcript_variant(ENST00000503252) non_coding_exon_variant(ENST00000503252) |
||
| 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.