ClinVar Genomic variation as it relates to human health
GRCh38/hg38 8p22(chr8:13544248-14757736)x3
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 | |||
C8orf48 | - | - | - |
GRCh38 GRCh37 |
- | - |
DLC1 | - | - |
GRCh38 GRCh38 GRCh37 |
- | - | |
LOC102725080 | - | - | - | GRCh38 | - | - |
LOC105379292 | - | - | - | GRCh38 | - | - |
LOC121294073 | - | - | - | GRCh38 | - | - |
LOC132089561 | - | - | - | GRCh38 | - | - |
LOC132089562 | - | - | - | GRCh38 | - | - |
LOC132089563 | - | - | - | GRCh38 | - | - |
LOC132089564 | - | - | - | GRCh38 | - | - |
LOC132089565 | - | - | - | GRCh38 | - | - |
There are 20 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
|
Likely benign (1) |
|
Sep 21, 2012 | RCV000139183.7 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024