ClinVar Genomic variation as it relates to human health
GRCh37/hg19 3p22.2-22.1(chr3:39373823-39531618)x3
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 | |||
CCR8 | - | - |
GRCh38 GRCh37 |
20 | 28 | |
MOBP | - | - |
GRCh38 GRCh37 |
10 | 18 | |
RPSA | - | - |
GRCh38 GRCh37 |
105 | 114 | |
SLC25A38 | - | - |
GRCh38 GRCh37 |
192 | 223 | |
SNORA62 | - | - |
GRCh38 GRCh37 |
- | 9 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Feb 1, 2024 | RCV003885503.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Aug 04, 2024