ClinVar Genomic variation as it relates to human health
GRCh38/hg38 7q34(chr7:142355688-142605368)x1
Germline
Classification
(1)
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 | |||
LOC126860208 | - | - | - |
GRCh38 GRCh38 |
- | 26 |
MIR11400 | - | - | - |
GRCh38 GRCh38 |
- | 26 |
TRB | - | - | - |
GRCh38 GRCh38 GRCh37 |
1 | 803 |
TRBV10-1 | - | - | - |
GRCh38 GRCh38 |
- | 25 |
TRBV10-2 | - | - | - |
GRCh38 GRCh38 |
- | 26 |
TRBV10-3 | - | - | - |
GRCh38 GRCh38 |
- | 28 |
TRBV11-1 | - | - | - |
GRCh38 GRCh38 |
- | 25 |
TRBV11-2 | - | - | - |
GRCh38 GRCh38 |
- | 26 |
TRBV11-3 | - | - | - |
GRCh38 GRCh38 |
- | 27 |
TRBV12-3 | - | - | - |
GRCh38 GRCh38 |
- | 27 |
There are 20 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Benign (1) |
|
Oct 1, 2010 | RCV000136743.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024