ClinVar Genomic variation as it relates to human health
GRCh38/hg38 15q25.3(chr15:85228050-85544770)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 | |||
AKAP13 | - | - |
GRCh38 GRCh37 |
210 | 257 | |
LOC112272622 | - | - | - | GRCh38 | - | 11 |
LOC126862205 | - | - | - | GRCh38 | - | 10 |
LOC130057826 | - | - | - | GRCh38 | - | 8 |
LOC130057827 | - | - | - | GRCh38 | - | 9 |
LOC130057828 | - | - | - | GRCh38 | - | 9 |
LOC130057829 | - | - | - | GRCh38 | - | 9 |
LOC130057830 | - | - | - | GRCh38 | - | 9 |
LOC130057831 | - | - | - | GRCh38 | - | 10 |
LOC130057832 | - | - | - | 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) |
|
Apr 30, 2011 | RCV000140612.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023