ClinVar Genomic variation as it relates to human health
NC_000003.11:g.(?_47079136)_(47454675_?)dup
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 | |||
SETD2 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
1171 | 1206 | |
KIF9 | - | - |
GRCh38 GRCh37 |
26 | 61 | |
KLHL18 | - | - |
GRCh38 GRCh37 |
25 | 43 | |
PTPN23 | - | - |
GRCh38 GRCh37 |
1342 | 1374 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Sep 6, 2022 | RCV003116703.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Sep 30, 2024