ClinVar Genomic variation as it relates to human health
GRCh37/hg19 17q12(chr17:34431767-34775684)x3
Germline
Classification
(1)
Likely benign
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 | |||
CCL3L1 | - | - |
GRCh38 GRCh37 |
4 | 28 | |
CCL3L3 | - | - |
GRCh38 GRCh38 GRCh38 GRCh37 |
1 | 38 | |
CCL4 | - | - |
GRCh38 GRCh38 GRCh38 GRCh37 |
3 | 21 | |
CCL4L1 | - | - |
GRCh38 GRCh37 |
- | 27 | |
CCL4L2 | - | - |
GRCh38 GRCh38 GRCh38 GRCh37 |
1 | 42 | |
TBC1D3B | - | - |
GRCh38 GRCh38 GRCh38 GRCh37 |
2 | 40 | |
TBC1D3C | - | - |
GRCh38 GRCh37 |
10 | 37 | |
TBC1D3H | - | - |
GRCh38 GRCh38 GRCh37 |
18 | 60 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Likely benign (1) |
|
Sep 21, 2012 | RCV000139674.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024