ClinVar Genomic variation as it relates to human health
GRCh38/hg38 18p11.32(chr18:1076081-1778651)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 | |||
LINC00470 | - | - | - | GRCh38 | - | 68 |
LOC112538442 | - | - | - | GRCh38 | - | 67 |
LOC125338462 | - | - | - | GRCh38 | 1 | 65 |
LOC129390952 | - | - | - | GRCh38 | - | 67 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
Aug 26, 2013 | RCV000142029.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024