ClinVar Genomic variation as it relates to human health
GRCh37/hg19 9q33.2-33.3(chr9:124604592-126306080)x1
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 | |||
CRB2 | - | - |
GRCh38 GRCh37 |
672 | 705 | |
DENND1A | - | - |
GRCh38 GRCh37 |
63 | 96 | |
GPR21 | - | - |
GRCh38 GRCh37 |
- | 55 | |
LHX6 | - | - |
GRCh38 GRCh37 |
13 | 41 | |
MORN5 | - | - |
GRCh38 GRCh37 |
11 | 41 | |
MRRF | - | - |
GRCh38 GRCh37 |
16 | 44 | |
NDUFA8 | - | - |
GRCh38 GRCh37 |
18 | 46 | |
OR1B1 | - | - | - |
GRCh38 GRCh37 |
21 | 52 |
OR1J1 | - | - | - |
GRCh38 GRCh37 |
- | 54 |
OR1J2 | - | - | - |
GRCh38 GRCh37 |
6 | 152 |
There are 20 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) |
|
Aug 15, 2018 | RCV001006270.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 26, 2023