ClinVar Genomic variation as it relates to human health
NC_000009.11:g.(?_94058283)_(94538120_?)dup
Germline
Classification
(2)
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 | |||
ROR2 | No evidence available | No evidence available |
GRCh38 GRCh37 |
676 | 716 | |
AUH | - | - |
GRCh38 GRCh37 |
191 | 273 | |
NFIL3 | - | - |
GRCh38 GRCh37 |
20 | 50 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
no classifications from unflagged records (1) |
|
- | RCV003107451.5 | |
Uncertain significance (1) |
|
Aug 22, 2022 | RCV003122563.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 09, 2023