ClinVar Genomic variation as it relates to human health
GRCh38/hg38 15q13.3(chr15:30969632-31317417)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 | |||
LINC02352 | - | - | - |
GRCh38 GRCh38 GRCh38 |
- | 91 |
LINC03034 | - | - | - |
GRCh38 GRCh38 GRCh38 |
- | 91 |
LOC110121498 | - | - | - |
GRCh38 GRCh38 GRCh38 |
- | 91 |
LOC112272582 | - | - | - |
GRCh38 GRCh38 GRCh38 |
- | 91 |
LOC121847941 | - | - | - |
GRCh38 GRCh38 GRCh38 |
- | 93 |
LOC126862088 | - | - | - |
GRCh38 GRCh38 GRCh38 |
- | 175 |
LOC126862089 | - | - | - |
GRCh38 GRCh38 GRCh38 |
- | 92 |
LOC128899998 | - | - | - |
GRCh38 GRCh38 GRCh38 |
- | 91 |
LOC128899999 | - | - | - |
GRCh38 GRCh38 GRCh38 |
- | 91 |
MIR211 | - | - |
GRCh38 GRCh38 GRCh38 GRCh37 |
- | 242 |
There are 2 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
|
Benign (1) |
|
Apr 30, 2011 | RCV000140616.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 26, 2023