HEX (Healthy Exomes)
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SNP Position | rsID | Alleles | Allele Count | Allele Number | Number of Homozygotes | Number of Heterozygotes | Hex MAF | ExAC MAF | Consequence | Annotation | Ensembl Transcript ID | Gene | Exon/Total Exons | Avg. Sample Read Depth |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
21:27543049 | rs459543 | C/G | 16 | 432 | 0 | 16 | 0.037 | upstream_gene_variant | ENST00000346798 | APP | 11.0764 | |||
21:27543049 | rs459543 | C/G | 16 | 432 | 0 | 16 | 0.037 | upstream_gene_variant | ENST00000608591 | AP000230.1 | 11.0764 | |||
21:27543049 | rs459543 | C/G | 16 | 432 | 0 | 16 | 0.037 | intron_variant&nc_transcript_variant | ENST00000455275 | AP001439.2 | 11.0764 |