ClinVar Genomic variation as it relates to human health
GRCh38/hg38 20q13.33(chr20:63095686-63524980)x1
Germline
Classification
(1)
Pathogenic
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 | |||
KCNQ2 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh38 GRCh37 |
2134 | 2265 | |
EEF1A2 | No evidence available | No evidence available |
GRCh38 GRCh37 |
497 | 658 | |
ARFGAP1 | - | - |
GRCh38 GRCh37 |
38 | 109 | |
BIRC7 | - | - |
GRCh38 GRCh37 |
26 | 92 | |
CHRNA4 | - | - |
GRCh38 GRCh37 |
877 | 1145 | |
COL20A1 | - | - |
GRCh38 GRCh37 |
126 | 197 | |
FLJ16779 | - | - | - | GRCh38 | - | 24 |
HAR1A | - | - |
GRCh38 GRCh37 |
- | 58 | |
HAR1B | - | - |
GRCh38 GRCh37 |
- | 58 | |
KCNQ2-AS1 | - | - | - | GRCh38 | - | 28 |
There are 29 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Pathogenic (1) |
|
Aug 12, 2011 | RCV000052771.4 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023