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- Data Summary
SNP Report
Name | rs9526970 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr13:53240546(Fwd) | ||
Variant Alleles | C/T | ||
Ancestral Allele | G | ||
Functional Annotation | downstream_gene_variant; intron_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000483074) intron_variant(ENST00000310528; ENST00000343788; ENST00000535397) |
||
No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
Source | LD-proxy |
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.