ClinVar Genomic variation as it relates to human health
NM_006736.6(DNAJB2):c.175+1G>C
Germline
Classification
(1)
Likely pathogenic
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 | |||
DNAJB2 | - | - |
GRCh38 GRCh37 |
282 | 321 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
DNAJB2-related disorder
|
Likely pathogenic (1) |
|
Feb 2, 2023 | RCV003412413.4 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 12, 2024