ClinVar Genomic variation as it relates to human health
GRCh38/hg38 6q23.2(chr6:132455272-133141153)x3
Germline
Classification
(1)
Uncertain significance
criteria provided, single submitter
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 | |||
LINC00326 | - | - | - | GRCh38 | - | 3 |
LOC123864071 | - | - | - | GRCh38 | - | 4 |
LOC126859792 | - | - | - | GRCh38 | - | 3 |
LOC126859793 | - | - | - | GRCh38 | - | 11 |
LOC126859794 | - | - | - | GRCh38 | - | 6 |
LOC126859795 | - | - | - | GRCh38 | - | 3 |
LOC129997172 | - | - | - | GRCh38 | - | 4 |
LOC129997173 | - | - | - | GRCh38 | - | 3 |
LOC129997174 | - | - | - | GRCh38 | - | 3 |
LOC129997175 | - | - | - | GRCh38 | - | 3 |
There are 26 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) |
|
Aug 12, 2011 | RCV000053388.4 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023