ClinVar Genomic variation as it relates to human health
GRCh38/hg38 8p23.3-23.1(chr8:782690-8222398)x3
Germline
Classification
(1)
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 | |||
CSMD1 | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
509 | 819 | |
DLGAP2 | No evidence available | No evidence available |
GRCh38 GRCh38 GRCh38 GRCh38 GRCh38 GRCh38 GRCh37 |
107 | 286 | |
AGPAT5 | - | - |
GRCh38 GRCh38 GRCh37 |
23 | 150 | |
ANGPT2 | - | - |
GRCh38 GRCh37 |
- | 237 | |
ARHGEF10 | - | - |
GRCh38 GRCh38 GRCh37 |
708 | 897 | |
CLN8 | - | - |
GRCh38 GRCh38 GRCh37 |
542 | 704 | |
CLN8-AS1 | - | - | - |
GRCh38 GRCh38 |
- | 62 |
DEFA1 | - | - |
GRCh38 GRCh38 GRCh37 |
- | 107 | |
DEFA1B | - | - | - |
GRCh38 GRCh38 GRCh37 |
- | 107 |
DEFA3 | - | - |
GRCh38 GRCh38 GRCh37 |
9 | 116 |
There are 153 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Benign (1) |
|
Sep 16, 2011 | RCV000137206.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024