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- Data Summary
SNP Report
Basic Info
| Name | rs576732 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr4:56237137(Fwd) | ||
| Variant Alleles | C/T | ||
| Ancestral Allele | T | ||
| Functional Annotation | 3_prime_UTR_variant; downstream_gene_variant; intron_variant; nc_transcript_variant. | ||
| Consequence to Transcript | 3_prime_UTR_variant(ENST00000264228) downstream_gene_variant(ENST00000505210; ENST00000592823; ENST00000514398) intron_variant(ENST00000433175; ENST00000595103; ENST00000510637; ENST00000596312; ENST00000595734; ENST00000598906; ENST00000596289) nc_transcript_variant(ENST00000433175; ENST00000595103; ENST00000510637; ENST00000596312; ENST00000595734; ENST00000596289; ENST00000598906) |
||
| No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
| Source | LD-proxy | ||
SNP related studies (count: 0)
SNP related genes (count: 2)
Literature-origin genes (count: 0)
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.