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- Data Summary
SNP Report
Basic Info
| Name | rs16940799 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr17:44102933(Fwd) | ||
| Variant Alleles | T/G/A/C | ||
| Ancestral Allele | T | ||
| Functional Annotation | 3_prime_UTR_variant; downstream_gene_variant. | ||
| Consequence to Transcript | 3_prime_UTR_variant(ENST00000446361; ENST00000535772; ENST00000262410; ENST00000351559; ENST00000344290; ENST00000340799; ENST00000347967) downstream_gene_variant(ENST00000334239; ENST00000415613; ENST00000571987; ENST00000420682; ENST00000574436; ENST00000431008; ENST00000576518; ENST00000576870; ENST00000574590; ENST00000572218; ENST00000575318; ENST00000262419; ENST00000572904; ENST00000432791; ENST00000393476) |
||
| No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
| Source | LD-proxy | ||
SNP related studies (count: 0)
SNP related genes (count: 3)
Literature-origin genes (count: 1)
Genes from other sources 
(count: 2)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.