ClinVar Genomic variation as it relates to human health
NM_018176.3(LGI2):c.-473617_-693dup
Germline
Classification
(1)
not provided
no classification 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 | |||
ANAPC4 | - | - |
GRCh38 GRCh37 |
- | - | |
LOC129992330 | - | - | - | GRCh38 | - | - |
LOC129992331 | - | - | - | GRCh38 | - | - |
LOC129992332 | - | - | - | GRCh38 | - | - |
LOC129992333 | - | - | - | GRCh38 | - | - |
LOC129992334 | - | - | - | GRCh38 | - | - |
LOC129992335 | - | - | - | GRCh38 | - | - |
LOC129992336 | - | - | - | GRCh38 | - | - |
LOC129992337 | - | - | - | GRCh38 | - | - |
LOC129992338 | - | - | - | GRCh38 | - | - |
There are 6 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
not provided (1) |
|
- | RCV000161338.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024