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SNP Report
| Name | rs11191447 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr10:102892566 - 102892566(1) | ||
| Variant Alleles | C/T | ||
| Ancestral Allele | C | ||
| Minor Allele | T | ||
| Minor Allele Frequence | 0.157149 | ||
| Functional Annotation | intron_variant; NMD_transcript_variant; upstream_gene_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000299353, ENST00000369880, ENST00000615257); NMD_transcript_variant(ENST00000299353); upstream_gene_variant(ENST00000438729) | ||
| No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||


