ClinVar Genomic variation as it relates to human health
NC_000015.9:g.(?_67546897)_(67571850_?)del
Germline
Classification
(1)
Pathogenic
criteria provided, single submitter
Somatic
No data submitted for somatic clinical impact
Somatic
No data submitted for oncogenicity
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
AAGAB | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
77 | 115 | |
IQCH | - | - |
GRCh38 GRCh37 |
42 | 85 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Pathogenic (1) |
|
Jul 27, 2022 | RCV001381833.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Sep 29, 2024