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- Data Summary
SNP Report
Basic Info
| Name | rs1810132 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr17:37866005(Fwd) | ||
| Variant Alleles | C/T | ||
| Ancestral Allele | T | ||
| Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
| Consequence to Transcript | NMD_transcript_variant(ENST00000578373; ENST00000582648) downstream_gene_variant(ENST00000578709; ENST00000584099) intron_variant(ENST00000445658; ENST00000583391; ENST00000584601; ENST00000582648; ENST00000584908; ENST00000582788; ENST00000269571; ENST00000578199; ENST00000578373; ENST00000583038; ENST00000584450; ENST00000406381; ENST00000541774; ENST00000540042; ENST00000540147) nc_transcript_variant(ENST00000583391; ENST00000584908; ENST00000582788; ENST00000583038) upstream_gene_variant(ENST00000578502) |
||
| 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.