ClinVar Genomic variation as it relates to human health
GRCh37/hg19 17q12(chr17:34158619-34477480)x4
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 | |||
CCL14 | - | - |
GRCh38 GRCh38 GRCh37 |
- | 13 | |
CCL15 | - | - |
GRCh38 GRCh38 GRCh37 |
- | 16 | |
CCL16 | - | - |
GRCh38 GRCh38 GRCh37 |
8 | 15 | |
CCL18 | - | - |
GRCh38 GRCh38 GRCh38 GRCh37 |
4 | 15 | |
CCL23 | - | - |
GRCh38 GRCh38 GRCh37 |
18 | 26 | |
CCL3 | - | - |
GRCh38 GRCh38 GRCh38 GRCh37 |
- | 16 | |
CCL4 | - | - |
GRCh38 GRCh38 GRCh38 GRCh37 |
3 | 21 | |
CCL5 | - | - |
GRCh38 GRCh38 GRCh37 |
6 | 13 | |
HEATR9 | - | - | - |
GRCh38 GRCh38 GRCh37 |
32 | 39 |
LYZL6 | - | - |
GRCh38 GRCh38 GRCh37 |
12 | 19 |
There are 2 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) |
|
Nov 8, 2018 | RCV001006895.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 26, 2023