ClinVar Genomic variation as it relates to human health
GRCh38/hg38 7q36.3(chr7:158858318-159135526)x3
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 | |||
DYNC2I1 | - | - |
GRCh38 GRCh37 |
474 | 601 | |
LINC00689 | - | - | - | GRCh38 | - | 55 |
LOC108254663 | - | - | - | GRCh38 | - | 55 |
LOC110121203 | - | - | - | GRCh38 | - | 58 |
LOC123956285 | - | - | - | GRCh38 | - | 54 |
LOC126860262 | - | - | - | GRCh38 | - | 56 |
LOC126860263 | - | - | - | GRCh38 | - | 58 |
LOC129999766 | - | - | - | GRCh38 | - | 55 |
VIPR2 | - | - |
GRCh38 GRCh37 |
40 | 161 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Benign (1) |
|
Jan 30, 2010 | RCV000133853.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024