ClinVar Genomic variation as it relates to human health
NC_000014.8:g.(?_20915399)_(22005055_?)dup
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 | |||
CHD8 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
1233 | 1333 | |
HNRNPC | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
13 | 63 | |
OR5AU1 | - | No evidence available | No evidence available |
GRCh38 GRCh37 |
19 | 58 |
SUPT16H | No evidence available | No evidence available |
GRCh38 GRCh37 |
74 | 134 | |
ANG | - | - |
GRCh38 GRCh37 |
8 | 124 | |
APEX1 | - | - |
GRCh38 GRCh38 GRCh37 |
19 | 48 | |
ARHGEF40 | - | - |
GRCh38 GRCh37 |
97 | 146 | |
EDDM3A | - | - |
GRCh38 GRCh37 |
13 | 42 | |
EDDM3B | - | - |
GRCh38 GRCh37 |
7 | 36 | |
METTL17 | - | - |
GRCh38 GRCh37 |
15 | 64 |
There are 30 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 |
---|---|---|---|---|
Uncertain significance (1) |
|
Jan 20, 2024 | RCV004578192.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Jun 30, 2024