ClinVar Genomic variation as it relates to human health
GRCh37/hg19 15q21.3(chr15:55346224-55967397)x3
Germline
Classification
(1)
Uncertain significance
criteria provided, single submitter
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 | |||
CCPG1 | - | - |
GRCh38 GRCh37 |
- | 101 | |
DNAAF4 | - | - |
GRCh38 GRCh37 |
21 | 313 | |
PIERCE2 | - | - |
GRCh38 GRCh37 |
- | 32 | |
PIGB | - | - |
GRCh38 GRCh37 |
278 | 359 | |
PRTG | - | - |
GRCh38 GRCh37 |
66 | 91 | |
PYGO1 | - | - |
GRCh38 GRCh37 |
20 | 46 | |
RAB27A | - | - |
GRCh38 GRCh37 |
302 | 333 | |
RSL24D1 | - | - |
GRCh38 GRCh37 |
10 | 31 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Aug 31, 2021 | RCV002475546.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 31, 2022