ClinVar Genomic variation as it relates to human health
GRCh37/hg19 20p13(chr20:2802218-4010802)x3
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 | |||
ADAM33 | - | - |
GRCh38 GRCh37 |
58 | 102 | |
AP5S1 | - | - |
GRCh38 GRCh37 |
21 | 63 | |
ATRN | - | - |
GRCh38 GRCh37 |
283 | 367 | |
AVP | - | - |
GRCh38 GRCh37 |
79 | 120 | |
C20orf27 | - | - | - |
GRCh38 GRCh37 |
- | 8 |
CDC25B | - | - |
GRCh38 GRCh37 |
18 | 70 | |
CENPB | - | - |
GRCh38 GRCh37 |
26 | 68 | |
DDRGK1 | - | - |
GRCh38 GRCh37 |
101 | 160 | |
DNAAF9 | - | - |
GRCh38 GRCh37 |
4 | 51 | |
FASTKD5 | - | - |
GRCh38 GRCh37 |
- | 88 |
There are 18 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Nov 4, 2019 | RCV001258752.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022