ClinVar Genomic variation as it relates to human health
GRCh37/hg19 14q11.2(chr14:20511672-21915516)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 | |||
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 | |
ANG | - | - |
GRCh38 GRCh37 |
8 | 123 | |
APEX1 | - | - |
GRCh38 GRCh38 GRCh37 |
19 | 47 | |
ARHGEF40 | - | - |
GRCh38 GRCh37 |
97 | 145 | |
CCNB1IP1 | - | - |
GRCh38 GRCh38 GRCh37 |
1 | 27 | |
EDDM3A | - | - |
GRCh38 GRCh37 |
13 | 41 | |
EDDM3B | - | - |
GRCh38 GRCh37 |
7 | 35 | |
HNRNPC | - | - |
GRCh38 GRCh37 |
12 | 59 |
There are 38 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) |
|
Feb 14, 2020 | RCV001259176.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 26, 2023