ClinVar Genomic variation as it relates to human health
GRCh38/hg38 17p13.3(chr17:162016-1904358)x1
Germline
Classification
(1)
Likely 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 | |||
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 | |
DOC2B | - | - |
GRCh38 GRCh38 GRCh37 |
24 | 77 | |
GEMIN4 | - | - |
GRCh38 GRCh37 |
171 | 277 | |
GLOD4 | - | - |
GRCh38 GRCh37 |
19 | 128 | |
INPP5K | - | - |
GRCh38 GRCh37 |
95 | 202 |
There are 94 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 |
---|---|---|---|---|
Likely pathogenic (1) |
|
Nov 11, 2011 | RCV000137940.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024