ClinVar Genomic variation as it relates to human health
GRCh38/hg38 15q26.2(chr15:94005151-95597885)x1
Germline
Classification
(1)
Uncertain significance
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 | |||
LETR1 | - | - | - | GRCh38 | - | 15 |
LINC00924 | - | - | - | GRCh38 | - | 15 |
LINC01581 | - | - | - | GRCh38 | - | 19 |
LOC105370987 | - | - | - | GRCh38 | - | 15 |
LOC105370993 | - | - | - | GRCh38 | - | 15 |
LOC112296177 | - | - | - | GRCh38 | - | 15 |
LOC125146359 | - | - | - | GRCh38 | - | 17 |
LOC126862231 | - | - | - | GRCh38 | - | 15 |
LOC126862232 | - | - | - | GRCh38 | - | 15 |
LOC129390738 | - | - | - | GRCh38 | - | 15 |
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
|
Uncertain significance (1) |
|
Mar 9, 2012 | RCV000138001.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024