ClinVar Genomic variation as it relates to human health
NC_000003.11:g.(?_197401889)_(197682644_?)del
Germline
Classification
(1)
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 | |||
FYTTD1 | - | - |
GRCh38 GRCh37 |
15 | 76 | |
IQCG | - | - |
GRCh38 GRCh37 |
29 | 208 | |
LRCH3 | - | - | - |
GRCh38 GRCh37 |
77 | 143 |
RPL35A | - | - |
GRCh38 GRCh37 |
- | 172 | |
RUBCN | - | - |
GRCh38 GRCh37 |
131 | 192 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Pathogenic (1) |
|
Feb 3, 2023 | RCV004582185.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Jul 07, 2024