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- Data Summary
SNP Report
Basic Info
| Name | rs17651549 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr17:44061278(Fwd) | ||
| Variant Alleles | C/G/T/A | ||
| Ancestral Allele | C | ||
| Functional Annotation | downstream_gene_variant; intron_variant; missense_variant; nc_transcript_variant; non_coding_exon_variant; synonymous_variant; upstream_gene_variant. | ||
| Consequence to Transcript | downstream_gene_variant(ENST00000572440) intron_variant(ENST00000334239; ENST00000446361; ENST00000570299; ENST00000420682; ENST00000574436; ENST00000340799; ENST00000431008; ENST00000576518; ENST00000351559; ENST00000535772; ENST00000347967) missense_variant(ENST00000571987; ENST00000415613; ENST00000344290; ENST00000262410) nc_transcript_variant(ENST00000570299; ENST00000576238) non_coding_exon_variant(ENST00000576238) synonymous_variant(ENST00000571987; ENST00000415613; ENST00000344290; ENST00000262410) upstream_gene_variant(ENST00000577017) |
||
| 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.