ClinVar Genomic variation as it relates to human health
GRCh37/hg19 14q11.2(chr14:20925965-23649548)x3
Germline
Classification
(1)
Likely 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 | |||
CHD8 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
1225 | 1321 | |
OR5AU1 | - | No evidence available | No evidence available |
GRCh38 GRCh37 |
19 | 57 |
SUPT16H | No evidence available | No evidence available |
GRCh38 GRCh37 |
73 | 128 | |
ABHD4 | - | - |
GRCh38 GRCh37 |
17 | 42 | |
ACIN1 | - | - |
GRCh38 GRCh37 |
63 | 95 | |
AJUBA | - | - |
GRCh38 GRCh37 |
22 | 44 | |
ANG | - | - |
GRCh38 GRCh37 |
8 | 123 | |
ARHGEF40 | - | - |
GRCh38 GRCh37 |
97 | 145 | |
C14orf119 | - | - | - |
GRCh38 GRCh37 |
- | 22 |
C14orf93 | - | - | - |
GRCh38 GRCh37 |
7 | 30 |
There are 52 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 |
---|---|---|---|---|
Likely pathogenic (1) |
|
Nov 1, 2021 | RCV001786536.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 02, 2023