ClinVar Genomic variation as it relates to human health
GRCh37/hg19 19q13.2-13.31(chr19:42891150-43922624)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 | |||
CD177 | - | - |
GRCh38 GRCh37 |
46 | 62 | |
CEACAM1 | - | - |
GRCh38 GRCh37 |
- | 21 | |
CEACAM8 | - | - |
GRCh38 GRCh37 |
- | 40 | |
CNFN | - | - |
GRCh38 GRCh37 |
1 | 14 | |
CXCL17 | - | - |
GRCh38 GRCh37 |
- | 13 | |
LIPE | - | - |
GRCh38 GRCh37 |
- | 189 | |
PRG1 | - | - |
GRCh38 GRCh37 |
- | 16 | |
PSG1 | - | - |
GRCh38 GRCh37 |
71 | 102 | |
PSG11 | - | - |
GRCh38 GRCh37 |
37 | 71 | |
PSG2 | - | - |
GRCh38 GRCh37 |
49 | 76 |
There are 8 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 |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
- | RCV000446399.4 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024