ClinVar Genomic variation as it relates to human health
GRCh37/hg19 2q12.2-21.2(chr2:106755586-134302739)x1
Germline
Classification
(1)
Pathogenic
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 | |||
GLI2 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
960 | 989 | |
PAX8 | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
105 | 223 | |
RABL2A | Dosage sensitivity unlikely | No evidence available |
GRCh38 GRCh37 |
16 | 31 | |
ARHGEF4 | No evidence available | No evidence available |
GRCh38 GRCh37 |
62 | 120 | |
BCL2L11 | No evidence available | No evidence available |
GRCh38 GRCh37 |
15 | 77 | |
CFC1 | No evidence available | No evidence available |
GRCh38 GRCh37 |
26 | 47 | |
CLASP1 | No evidence available | No evidence available |
GRCh38 GRCh37 |
57 | 326 | |
GPR148 | - | No evidence available | No evidence available |
GRCh38 GRCh37 |
32 | 87 |
ACOXL | - | - | - |
GRCh38 GRCh37 |
37 | 105 |
ACTR3 | - | - |
GRCh38 GRCh37 |
8 | 24 |
There are 113 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Pathogenic (1) |
|
- | RCV003986380.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 30, 2024