ClinVar Genomic variation as it relates to human health
GRCh38/hg38 20q13.33(chr20:61262566-61742628)x1
Germline
Classification
(1)
Uncertain significance
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 | |||
CDH4 | - | - |
GRCh38 GRCh38 GRCh37 |
113 | 137 | |
LOC100128310 | - | - | - |
GRCh38 GRCh37 |
- | 21 |
LOC105372703 | - | - | - | GRCh38 | - | 10 |
LOC125387313 | - | - | - | GRCh38 | - | 10 |
LOC126863077 | - | - | - | GRCh38 | - | 10 |
LOC126863078 | - | - | - | GRCh38 | - | 10 |
LOC126863079 | - | - | - | GRCh38 | - | 10 |
LOC129391206 | - | - | - | GRCh38 | - | 11 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
Sep 30, 2011 | RCV000137811.7 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024