ClinVar Genomic variation as it relates to human health
NM_015898.4(ZBTB7A):c.26T>G (p.Ile9Ser)
Germline
Classification
(1)
Uncertain significance
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 | |||
ZBTB7A | - | - |
GRCh38 GRCh37 |
66 | 95 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
ZBTB7A-related disorder
|
Uncertain significance (1) |
|
Jul 17, 2023 | RCV003416730.4 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 27, 2024