ClinVar Genomic variation as it relates to human health
GRCh37/hg19 4q13.3(chr4:74846849-74964907)x3
Germline
Classification
(1)
Likely benign
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 | |||
CXCL2 | - | - |
GRCh38 GRCh37 |
2 | 29 | |
CXCL3 | - | - |
GRCh38 GRCh37 |
5 | 29 | |
CXCL5 | - | - |
GRCh38 GRCh37 |
4 | 27 | |
PF4 | - | - |
GRCh38 GRCh37 |
6 | 29 | |
PPBP | - | - |
GRCh38 GRCh37 |
3 | 26 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
- | RCV000448541.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022