ClinVar Genomic variation as it relates to human health
GRCh38/hg38 15q26.3(chr15:98976591-99598500)x3
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 | |||
LINC02244 | - | - | - | GRCh38 | - | 34 |
LOC105371017 | - | - | - | GRCh38 | - | 34 |
LOC125146367 | - | - | - | GRCh38 | - | 32 |
LOC126862246 | - | - | - | GRCh38 | - | 35 |
LOC126862247 | - | - | - | GRCh38 | - | 34 |
LOC129390743 | - | - | - | GRCh38 | - | 34 |
LOC129390744 | - | - | - | GRCh38 | - | 34 |
LOC130058007 | - | - | - | GRCh38 | - | 35 |
LOC130058008 | - | - | - | GRCh38 | - | 35 |
LOC130058009 | - | - | - | GRCh38 | - | 35 |
There are 27 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) |
|
Jun 18, 2012 | RCV000138661.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024