ClinVar Genomic variation as it relates to human health
GRCh37/hg19 4q28.3-31.21(chr4:134054911-142601496)x1
Germline
Classification
(1)
Uncertain significance
no assertion criteria provided
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 | |||
NAA15 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
372 | 416 | |
CLGN | - | - |
GRCh38 GRCh37 |
36 | 70 | |
ELF2 | - | - |
GRCh38 GRCh37 |
18 | 52 | |
ELMOD2 | - | - |
GRCh38 GRCh37 |
30 | 63 | |
IL15 | - | - |
GRCh38 GRCh37 |
10 | 42 | |
MAML3 | - | - |
GRCh38 GRCh37 |
23 | 57 | |
MGARP | - | - |
GRCh38 GRCh37 |
5 | 48 | |
MGAT4D | - | - |
GRCh38 GRCh37 |
- | 33 | |
MGST2 | - | - |
GRCh38 GRCh37 |
9 | 42 | |
NDUFC1 | - | - |
GRCh38 GRCh37 |
8 | 53 |
There are 12 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Mar 30, 2018 | RCV000847693.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 11, 2022