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- Data Summary
SNP Report
Basic Info
| Name | rs260452 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr19:58766874(Fwd) | ||
| Variant Alleles | A/C | ||
| Ancestral Allele | C | ||
| Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant. | ||
| Consequence to Transcript | NMD_transcript_variant(ENST00000596677; ENST00000600029) downstream_gene_variant(ENST00000597230; ENST00000333581) intron_variant(ENST00000596677; ENST00000415203; ENST00000595981; ENST00000598880; ENST00000594384; ENST00000596652; ENST00000600220; ENST00000596929; ENST00000600044; ENST00000599953; ENST00000596825; ENST00000599227; ENST00000269829; ENST00000600029) nc_transcript_variant(ENST00000598880) |
||
| 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: 1)
Genes from other sources 
(count: 0)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.