ClinVar Genomic variation as it relates to human health
GRCh38/hg38 15q26.3(chr15:101621277-101708810)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 | |||
LOC130058078 | - | - | - | GRCh38 | - | 39 |
LOC130058079 | - | - | - | GRCh38 | - | 46 |
LOC130058080 | - | - | - | GRCh38 | - | 40 |
TARS3 | - | - | - |
GRCh38 GRCh37 |
51 | 158 |
TM2D3 | - | - |
GRCh38 GRCh37 |
16 | 122 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Benign (1) |
|
Jul 1, 2013 | RCV000133748.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024