ClinVar Genomic variation as it relates to human health
NM_001029883.3(PCARE):c.3673_3675dupAGC
Germline
Classification
(5)
Benign/Likely benign
criteria provided, multiple submitters, no conflicts
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 | |||
PCARE | - | - |
GRCh38 GRCh37 |
1073 | 1100 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Jun 14, 2016 | RCV000278051.14 | |
Benign (1) |
|
Apr 14, 2016 | RCV000382560.13 | |
Benign (1) |
|
May 28, 2019 | RCV000986607.10 | |
Benign (1) |
|
Jan 31, 2024 | RCV001511102.15 | |
Benign (1) |
|
Oct 1, 2023 | RCV003888792.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 17, 2024