ClinVar Genomic variation as it relates to human health
GRCh38/hg38 15q25.2(chr15:83598551-84060830)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 | |||
ADAMTSL3 | - | - |
GRCh38 GRCh38 GRCh37 |
197 | 239 | |
LOC126862204 | - | - | - |
GRCh38 GRCh38 |
- | 8 |
LOC130057791 | - | - | - |
GRCh38 GRCh38 |
- | 9 |
LOC130057792 | - | - | - |
GRCh38 GRCh38 |
- | 9 |
LOC130057793 | - | - | - |
GRCh38 GRCh38 |
- | 9 |
LOC130057794 | - | - | - |
GRCh38 GRCh38 |
- | 9 |
LOC130057795 | - | - | - |
GRCh38 GRCh38 |
- | 9 |
LOC130057796 | - | - | - |
GRCh38 GRCh38 |
- | 9 |
LOC130057797 | - | - | - |
GRCh38 GRCh38 |
- | 9 |
LOC130057798 | - | - | - |
GRCh38 GRCh38 |
- | 9 |
There are 16 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 |
---|---|---|---|---|
See cases
|
Likely benign (1) |
|
Nov 30, 2010 | RCV000136088.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024