ClinVar Genomic variation as it relates to human health
GRCh37/hg19 8q23.2-24.13(chr8:111514791-123192373)x1
Germline
Classification
(1)
Pathogenic
no assertion criteria provided
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 | |||
EXT1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
958 | 1029 | |
RAD21 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
355 | 416 | |
TRPS1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
599 | 659 | |
AARD | - | - | - |
GRCh38 GRCh37 |
4 | 61 |
CCN3 | - | - |
GRCh38 GRCh37 |
16 | 74 | |
COL14A1 | - | - |
GRCh38 GRCh37 |
203 | 253 | |
COLEC10 | - | - |
GRCh38 GRCh37 |
20 | 84 | |
CSMD3 | - | - |
GRCh38 GRCh37 |
256 | 305 | |
DEPTOR | - | - |
GRCh38 GRCh37 |
23 | 83 | |
DSCC1 | - | - |
GRCh38 GRCh37 |
16 | 74 |
There are 15 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Pathogenic (1) |
|
Jan 3, 2019 | RCV001006131.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 26, 2023