ClinVar Genomic variation as it relates to human health
GRCh38/hg38 5q35.2-35.3(chr5:176132340-177586960)x1
Germline
Classification
(2)
Pathogenic
criteria provided, multiple submitters, no conflicts
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 | |||
DDX41 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
529 | - | |
NSD1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
1656 | - | |
ARL10 | - | - | - |
GRCh38 GRCh37 |
- | - |
CDHR2 | - | - |
GRCh38 GRCh37 |
68 | - | |
CLTB | - | - |
GRCh38 GRCh37 |
- | 55 | |
DBN1 | - | - |
GRCh38 GRCh37 |
32 | 95 | |
DOK3 | - | - |
GRCh38 GRCh37 |
- | 107 | |
EIF4E1B | - | - | - |
GRCh38 GRCh37 |
- | 70 |
F12 | - | - |
GRCh38 GRCh37 |
126 | 218 | |
FAF2 | - | - |
GRCh38 GRCh37 |
- | - |
There are 121 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Pathogenic (2) |
|
Aug 12, 2011 | RCV000050645.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023