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SNP Report
| Name | rs4851142 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr2:98517148 - 98517148(1) | ||
| Variant Alleles | A/C | ||
| Ancestral Allele | A | ||
| Minor Allele | C | ||
| Minor Allele Frequence | 0.263379 | ||
| Functional Annotation | intron_variant; upstream_gene_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000074304, ENST00000409016, ENST00000409463, ENST00000409540, ENST00000409851); upstream_gene_variant(ENST00000463367, ENST00000523221) | ||
| No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||


