ClinVar Genomic variation as it relates to human health
GRCh38/hg38 17p13.1(chr17:6958978-7491129)x3
Germline
Classification
(1)
Uncertain significance
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 |
141 | 303 | |
ACADVL | - | - |
GRCh38 GRCh37 |
1708 | 1913 | |
ACAP1 | - | - |
GRCh38 GRCh38 GRCh37 |
41 | 75 | |
ALOX12 | - | - |
GRCh38 GRCh37 |
- | 91 | |
ALOX12-AS1 | - | - | - | GRCh38 | - | 79 |
ASGR1 | - | - |
GRCh38 GRCh37 |
11 | 40 | |
ASGR2 | - | - |
GRCh38 GRCh37 |
22 | 49 | |
BCL6B | - | - |
GRCh38 GRCh37 |
10 | 33 | |
C17orf49 | - | - |
GRCh38 GRCh37 |
- | 23 | |
CHRNB1 | - | - |
GRCh38 GRCh38 GRCh37 |
460 | 506 |
There are 98 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 |
---|---|---|---|---|
Uncertain significance (1) |
|
Feb 28, 2010 | RCV000133763.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024