ClinVar Genomic variation as it relates to human health
GRCh38/hg38 3q26.32(chr3:177511733-178172084)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 | |||
LINC00578 | - | - | - | GRCh38 | - | 15 |
LINC02015 | - | - | - | GRCh38 | - | 15 |
LOC105374235 | - | - | - | GRCh38 | - | 15 |
LOC121725164 | - | - | - | GRCh38 | - | 15 |
LOC123256949 | - | - | - | GRCh38 | - | 14 |
LOC123256950 | - | - | - | GRCh38 | - | 14 |
LOC129389177 | - | - | - | GRCh38 | - | 14 |
LOC129389178 | - | - | - | GRCh38 | - | 14 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Oct 23, 2012 | RCV000143110.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024