ClinVar Genomic variation as it relates to human health
GRCh38/hg38 17p13.3(chr17:234496-2385512)x3
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 | |||
ABR | No evidence available | No evidence available |
GRCh38 GRCh38 GRCh38 GRCh37 |
48 | 174 | |
PITPNA | No evidence available | No evidence available |
GRCh38 GRCh37 |
6 | 109 | |
YWHAE | No evidence available | No evidence available |
GRCh38 GRCh38 GRCh37 |
69 | 206 | |
ABR-AS1 | - | - | - |
GRCh38 GRCh38 |
- | 38 |
BHLHA9 | - | - |
GRCh38 GRCh37 |
57 | 181 | |
CRK | - | - |
GRCh38 GRCh38 GRCh37 |
12 | 124 | |
DPH1 | - | - |
GRCh38 GRCh37 |
94 | 190 | |
GEMIN4 | - | - |
GRCh38 GRCh37 |
171 | 277 | |
GLOD4 | - | - |
GRCh38 GRCh37 |
19 | 128 | |
HIC1 | - | - |
GRCh38 GRCh37 |
19 | 117 |
There are 170 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Pathogenic (1) |
|
Aug 12, 2011 | RCV000052429.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024