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- Data Summary
SNP Report
Basic Info
| Name | rs16965663 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr17:28601005(Fwd) | ||
| Variant Alleles | G/A | ||
| Ancestral Allele | G | ||
| Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant. | ||
| Consequence to Transcript | NMD_transcript_variant(ENST00000578090) intron_variant(ENST00000581037; ENST00000584603; ENST00000261714; ENST00000578090; ENST00000577623; ENST00000394819; ENST00000582669) nc_transcript_variant(ENST00000582669; ENST00000579325) non_coding_exon_variant(ENST00000579325) upstream_gene_variant(ENST00000579957; ENST00000577306) |
||
| 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.