ClinVar Genomic variation as it relates to human health
NM_005807.6(PRG4):c.713C>T (p.Thr238Met)
Germline
Classification
(1)
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 | |||
PRG4 | - | - |
GRCh38 GRCh37 |
177 | 220 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
PRG4-related disorder
|
Benign (1) |
|
Apr 12, 2019 | RCV003914113.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 08, 2024