ClinVar Genomic variation as it relates to human health
GRCh38/hg38 15q26.3(chr15:101552822-101843270)x1
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 | |||
LINC02348 | - | - | - | GRCh38 | - | 36 |
LOC126862257 | - | - | - | GRCh38 | - | 35 |
LOC126862258 | - | - | - | GRCh38 | - | 34 |
LOC126862259 | - | - | - | GRCh38 | - | 30 |
LOC129390750 | - | - | - | GRCh38 | - | 35 |
LOC130058078 | - | - | - | GRCh38 | - | 39 |
LOC130058079 | - | - | - | GRCh38 | - | 46 |
LOC130058080 | - | - | - | GRCh38 | - | 40 |
LOC130058081 | - | - | - | GRCh38 | - | 40 |
LOC130058082 | - | - | - | GRCh38 | - | 34 |
There are 4 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 | RCV000142767.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024