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            SNP Report
| Name | rs12474624 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr2:159440061 - 159440061(1) | ||
| Variant Alleles | C/T | ||
| Ancestral Allele | C | ||
| Minor Allele | T | ||
| Minor Allele Frequence | 0.241613 | ||
| Functional Annotation | intron_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000343439, ENST00000392782, ENST00000392783, ENST00000467184, ENST00000482503); non_coding_transcript_variant(ENST00000467184, ENST00000482503); upstream_gene_variant(ENST00000472953, ENST00000605196) | ||
| No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||



