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- Data Summary
SNP Report
Basic Info
| Name | rs2002739 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr15:91452106(Fwd) | ||
| Variant Alleles | C/T | ||
| Ancestral Allele | C | ||
| Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
| Consequence to Transcript | NMD_transcript_variant(ENST00000560451; ENST00000558161) downstream_gene_variant(ENST00000559999; ENST00000558853; ENST00000559965; ENST00000558640; ENST00000558290; ENST00000561046; ENST00000559132) intron_variant(ENST00000560451; ENST00000560616; ENST00000431652; ENST00000557865; ENST00000559717; ENST00000560192; ENST00000558161; ENST00000360468) nc_transcript_variant(ENST00000560192) upstream_gene_variant(ENST00000561047; ENST00000561240; ENST00000557990; ENST00000560505; ENST00000559374; ENST00000558171; ENST00000430376; ENST00000560147; ENST00000561448) |
||
| 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.