ClinVar Genomic variation as it relates to human health
GRCh37/hg19 8q24.3(chr8:142836592-144175046)x1
Germline
Classification
(1)
Uncertain significance
criteria provided, single submitter
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 | |||
ADGRB1 | - | - |
GRCh38 GRCh37 |
82 | 144 | |
ARC | - | - |
GRCh38 GRCh37 |
10 | 68 | |
CYP11B1 | - | - |
GRCh38 GRCh37 |
207 | 889 | |
CYP11B2 | - | - |
GRCh38 GRCh37 |
19 | 729 | |
GML | - | - |
GRCh38 GRCh37 |
11 | 78 | |
JRK | - | - |
GRCh38 GRCh37 |
31 | 92 | |
LINC02904 | - | - | - |
GRCh38 GRCh38 GRCh37 |
- | 11 |
LY6D | - | - |
GRCh38 GRCh37 |
6 | 72 | |
LY6E | - | - |
GRCh38 GRCh38 GRCh37 |
13 | 75 | |
LY6K | - | - |
GRCh38 GRCh37 |
8 | 79 |
There are 6 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Jun 23, 2022 | RCV002473674.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 31, 2022