ClinVar Genomic variation as it relates to human health
GRCh38/hg38 11q24.3-25(chr11:130457291-133168833)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 | |||
ADAMTS15 | - | - |
GRCh38 GRCh37 |
72 | 153 | |
LINC02551 | - | - | - | GRCh38 | - | 39 |
LINC02873 | - | - | - |
GRCh38 GRCh37 |
- | 80 |
LOC101929653 | - | - | - | GRCh38 | - | 38 |
LOC108165612 | - | - | - | GRCh38 | - | 37 |
LOC108165613 | - | - | - | GRCh38 | - | 38 |
LOC110120853 | - | - | - | GRCh38 | - | 39 |
LOC121392952 | - | - | - | GRCh38 | - | 39 |
LOC121392953 | - | - | - | GRCh38 | - | 39 |
LOC124625872 | - | - | - | GRCh38 | - | 38 |
There are 35 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 |
---|---|---|---|---|
Uncertain significance (1) |
|
Jul 18, 2014 | RCV000143289.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024