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- Data Summary
SNP Report
Basic Info
| Name | rs1450900 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr4:62763217(Fwd) | ||
| Variant Alleles | C/T | ||
| Ancestral Allele | T | ||
| Functional Annotation | intron_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000512091; ENST00000511324; ENST00000514591; ENST00000509896; ENST00000506700; ENST00000507164; ENST00000507625; ENST00000508693; ENST00000514157; ENST00000508946; ENST00000504896; ENST00000502815; ENST00000506720; ENST00000514996; ENST00000506746; ENST00000545650; ENST00000570545; ENST00000574812; ENST00000574919; ENST00000573738; ENST00000577151; ENST00000572342; ENST00000576325; ENST00000573960; ENST00000576469; ENST00000572079; ENST00000574839; ENST00000576028; ENST00000574536; ENST00000571630; ENST00000573720) | ||
| 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.