ClinVar Genomic variation as it relates to human health
GRCh38/hg38 17p13.3-12(chr17:150732-14764202)x3
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 | |||
DLG4 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
139 | 297 | |
PAFAH1B1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
520 | 603 | |
TP53 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
3195 | 3292 | |
KDM6B | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
400 | 502 | |
MYH10 | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
124 | 155 | |
ABR | No evidence available | No evidence available |
GRCh38 GRCh38 GRCh38 GRCh37 |
69 | 200 | |
PITPNA | No evidence available | No evidence available |
GRCh38 GRCh37 |
3 | 112 | |
YWHAE | No evidence available | No evidence available |
GRCh38 GRCh38 GRCh37 |
68 | 204 | |
ABR-AS1 | - | - | - |
GRCh38 GRCh38 |
- | 38 |
ACADVL | - | - |
GRCh38 GRCh37 |
1703 | 1910 |
There are 955 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) |
|
Mar 10, 2014 | RCV000142236.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023