ClinVar Genomic variation as it relates to human health
NM_000294.3(PHKG2):c.392+10G>A
Germline
Classification
(2)
Likely benign
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 | |||
PHKG2 | - | - |
GRCh38 GRCh37 |
365 | 426 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Apr 14, 2023 | RCV003628024.2 | |
PHKG2-related disorder
|
Likely benign (1) |
|
Oct 15, 2020 | RCV003901257.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 13, 2024