ClinVar Genomic variation as it relates to human health
GRCh38/hg38 8q24.22(chr8:132935590-133815152)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 | |||
CCN4 | - | - |
GRCh38 GRCh37 |
39 | 101 | |
LINC03024 | - | - | - | GRCh38 | - | 25 |
LOC101927798 | - | - | - | GRCh38 | - | 25 |
LOC124188237 | - | - | - | GRCh38 | - | 25 |
LOC126860527 | - | - | - | GRCh38 | - | 25 |
LOC126860528 | - | - | - | GRCh38 | - | 25 |
LOC126860529 | - | - | - | GRCh38 | - | 25 |
LOC126860530 | - | - | - | GRCh38 | - | 25 |
LOC126860531 | - | - | - | GRCh38 | - | 111 |
LOC126860532 | - | - | - | GRCh38 | - | 25 |
There are 31 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 |
---|---|---|---|---|
Uncertain significance (1) |
|
Jul 22, 2013 | RCV000143529.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024