ClinVar Genomic variation as it relates to human health
GRCh37/hg19 9p13.3(chr9:34247282-34986900)x4
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 | |||
ARID3C | - | - | - |
GRCh38 GRCh37 |
24 | 99 |
C9orf24 | - | - |
GRCh38 GRCh37 |
- | 2 | |
CCL19 | - | - |
GRCh38 GRCh37 |
- | 82 | |
CCL21 | - | - |
GRCh38 GRCh37 |
- | 85 | |
CCL27 | - | - |
GRCh38 GRCh37 |
7 | 83 | |
CNTFR | - | - |
GRCh38 GRCh37 |
14 | 90 | |
DCTN3 | - | - |
GRCh38 GRCh37 |
12 | 87 | |
DNAI1 | - | - |
GRCh38 GRCh37 |
880 | 961 | |
ENHO | - | - |
GRCh38 GRCh37 |
- | 74 | |
FAM205A | - | - | - |
GRCh38 GRCh37 |
- | 3 |
There are 10 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
May 23, 2022 | RCV002473496.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 31, 2022