最新の情報は下記 URL でご確認いただけます (外部サイトへ移動します) 。
https://ftp.ncbi.nlm.nih.gov/pub/clinvar/tab_delimited/archive/
表のタイトル行が青色の項目は、クリックすることでソートすることができます。
| Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
|---|---|---|---|---|---|---|---|---|---|---|
| (GRCh37) | ||||||||||
| single nucleotide variant | NM_000018.4(ACADVL):c.205-2A>G | ACADVL | Likely pathogenic | 17 | 7123921 | 7123921 | A | G | criteria provided, single submitter | - |
| single nucleotide variant | NM_000018.4(ACADVL):c.139-1G>T | ACADVL | Likely pathogenic | 17 | 7123782 | 7123782 | G | T | criteria provided, single submitter | - |
| single nucleotide variant | NM_000018.4(ACADVL):c.1605+2T>C | ACADVL | Likely pathogenic | 17 | 7127714 | 7127714 | T | C | reviewed by expert panel | - |