ClinVar Genomic variation as it relates to human health
GRCh37/hg19 3p26.2-25.3(chr3:3691505-9917651)x1
Germline
Classification
(1)
Pathogenic
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 | |||
BRPF1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
309 | 367 | |
SETD5 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
1006 | 1073 | |
ITPR1 | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
1679 | 1879 | |
ARL8B | - | - |
GRCh38 GRCh37 |
1 | 91 | |
ARPC4 | - | - |
GRCh38 GRCh37 |
- | 62 | |
ARPC4-TTLL3 | - | - | - |
GRCh38 GRCh37 |
- | 151 |
BHLHE40 | - | - |
GRCh38 GRCh37 |
17 | 105 | |
CAMK1 | - | - |
GRCh38 GRCh37 |
- | 78 | |
CAV3 | - | - |
GRCh38 GRCh37 |
100 | 441 | |
CIDEC | - | - |
GRCh38 GRCh37 |
44 | 107 |
There are 21 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) |
|
Sep 27, 2023 | RCV003330127.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 02, 2023