ClinVar Genomic variation as it relates to human health
GRCh37/hg19 8q24.3(chr8:142988974-144218537)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 | |||
ADGRB1 | - | - |
GRCh38 GRCh37 |
93 | 157 | |
ARC | - | - |
GRCh38 GRCh37 |
11 | 69 | |
CYP11B1 | - | - |
GRCh38 GRCh37 |
210 | 903 | |
CYP11B2 | - | - |
GRCh38 GRCh37 |
19 | 737 | |
GML | - | - |
GRCh38 GRCh37 |
11 | 78 | |
JRK | - | - |
GRCh38 GRCh37 |
35 | 96 | |
LINC02904 | - | - | - |
GRCh38 GRCh38 GRCh37 |
- | 11 |
LY6D | - | - |
GRCh38 GRCh37 |
7 | 73 | |
LY6E | - | - |
GRCh38 GRCh38 GRCh37 |
13 | 75 | |
LY6K | - | - |
GRCh38 GRCh37 |
9 | 81 |
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) |
|
Sep 11, 2017 | RCV000846118.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 11, 2022