ClinVar Genomic variation as it relates to human health
GRCh38/hg38 13q32.2-32.3(chr13:97674476-99498445)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 | |||
DOCK9 | - | - |
GRCh38 GRCh37 |
102 | 204 | |
DOCK9-AS1 | - | - | - | GRCh38 | - | 30 |
DOCK9-DT | - | - | - | GRCh38 | - | 30 |
FARP1 | - | - |
GRCh38 GRCh37 |
66 | 195 | |
FARP1-AS1 | - | - | - | GRCh38 | - | 33 |
FKSG29 | - | - | - | GRCh38 | - | 30 |
GPR18 | - | - |
GRCh38 GRCh37 |
- | 114 | |
GPR183 | - | - |
GRCh38 GRCh37 |
- | 110 | |
IPO5 | - | - |
GRCh38 GRCh37 |
6 | 93 | |
LINC01232 | - | - | - | GRCh38 | - | 31 |
There are 90 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
Aug 12, 2011 | RCV000052030.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023