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SNP Report
| Name | rs13026780 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr2:159456400 - 159456400(1) | ||
| Variant Alleles | T/C | ||
| Ancestral Allele | T | ||
| Minor Allele | C | ||
| Minor Allele Frequence | 0.241813 | ||
| Functional Annotation | downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
| Consequence to Transcript | downstream_gene_variant(ENST00000483316); intron_variant(ENST00000392782, ENST00000392783, ENST00000437839, ENST00000467184, ENST00000482503, ENST00000541068); non_coding_transcript_variant(ENST00000467184, ENST00000482503); upstream_gene_variant(ENST00000343439) | ||
| No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||


