ClinVar Genomic variation as it relates to human health
GRCh38/hg38 7q34(chr7:142620494-142732123)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 | |||
LOC121201615 | - | - | - |
GRCh38 GRCh38 |
- | 31 |
LOC123956253 | - | - | - |
GRCh38 GRCh38 |
- | 33 |
LOC123956254 | - | - | - |
GRCh38 GRCh38 |
- | 31 |
LOC129389904 | - | - | - |
GRCh38 GRCh38 |
- | 31 |
MTRNR2L6 | - | - | - |
GRCh38 GRCh38 GRCh37 |
- | 61 |
TRB | - | - | - |
GRCh38 GRCh38 GRCh37 |
1 | 803 |
TRBV20-1 | - | - | - |
GRCh38 GRCh38 |
- | 31 |
TRBV24-1 | - | - | - |
GRCh38 GRCh38 |
- | 31 |
TRBV25-1 | - | - | - |
GRCh38 GRCh38 |
- | 31 |
TRBV27 | - | - | - |
GRCh38 GRCh38 |
- | 32 |
There is 1 more gene 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) |
|
Nov 30, 2010 | RCV000135131.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023