ClinVar Genomic variation as it relates to human health
GRCh38/hg38 16p13.12(chr16:14140498-14686337)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 | |||
BFAR | - | - |
GRCh38 GRCh38 GRCh37 |
30 | 57 | |
LINC02130 | - | - | - | GRCh38 | - | 5 |
LOC111464986 | - | - | - |
GRCh38 GRCh38 |
- | 5 |
LOC111822950 | - | - | - | GRCh38 | - | 5 |
LOC111822951 | - | - | - |
GRCh38 GRCh38 |
- | 5 |
LOC112296189 | - | - | - | GRCh38 | - | 5 |
LOC113939948 | - | - | - | GRCh38 | - | 5 |
LOC125146416 | - | - | - | GRCh38 | - | 5 |
LOC125146417 | - | - | - |
GRCh38 GRCh38 |
- | 5 |
LOC126862297 | - | - | - | GRCh38 | - | 10 |
There are 19 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) |
|
Oct 10, 2011 | RCV000137490.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024