ClinVar Genomic variation as it relates to human health
GRCh38/hg38 12q24.33(chr12:132966304-133202490)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 | |||
LOC126861702 | - | - | - | GRCh38 | - | 25 |
LOC129390595 | - | - | - | GRCh38 | - | 11 |
LOC130009282 | - | - | - | GRCh38 | - | 11 |
LOC130009283 | - | - | - | GRCh38 | - | 11 |
LOC130009284 | - | - | - | GRCh38 | - | 11 |
LOC130009285 | - | - | - | GRCh38 | - | 11 |
LOC130009286 | - | - | - | GRCh38 | - | 11 |
LOC130009287 | - | - | - | GRCh38 | - | 12 |
LOC130009288 | - | - | - | GRCh38 | - | 12 |
LOC130009289 | - | - | - | GRCh38 | - | 12 |
There are 10 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 |
---|---|---|---|---|
Likely benign (1) |
|
Aug 5, 2011 | RCV000137311.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024