ClinVar Genomic variation as it relates to human health
GRCh38/hg38 15q14(chr15:34334908-34549221)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 | |||
GOLGA8A | - | - |
GRCh38 GRCh38 GRCh37 |
23 | 59 | |
GOLGA8B | - | - |
GRCh38 GRCh37 |
16 | 47 | |
LOC126862098 | - | - | - | GRCh38 | - | 18 |
LOC130056745 | - | - | - |
GRCh38 GRCh38 |
- | 10 |
LOC130056746 | - | - | - |
GRCh38 GRCh38 |
- | 10 |
LOC130056747 | - | - | - |
GRCh38 GRCh38 |
- | 10 |
LOC130056748 | - | - | - |
GRCh38 GRCh38 |
- | 10 |
LOC130056749 | - | - | - |
GRCh38 GRCh38 |
- | 10 |
LOC130056750 | - | - | - |
GRCh38 GRCh38 |
- | 15 |
LOC130056751 | - | - | - |
GRCh38 GRCh38 |
- | 10 |
There are 13 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 | RCV000138654.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024