ClinVar Genomic variation as it relates to human health
GRCh37/hg19 8p23.3(chr8:406041-695480)x1
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 | |||
ERICH1 | - | - | - |
GRCh38 GRCh38 GRCh37 |
58 | 206 |
FBXO25 | - | - |
GRCh38 GRCh37 |
25 | 176 | |
TDRP | - | - |
GRCh38 GRCh37 |
24 | 172 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Feb 22, 2023 | RCV003483002.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Feb 04, 2024