ClinVar Genomic variation as it relates to human health
GRCh37/hg19 17p13.3(chr17:1-2538512)x4,5
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 | |||
PAFAH1B1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
520 | 603 | |
ABR | No evidence available | No evidence available |
GRCh38 GRCh38 GRCh38 GRCh37 |
34 | 160 | |
PITPNA | No evidence available | No evidence available |
GRCh38 GRCh37 |
3 | 106 | |
YWHAE | No evidence available | No evidence available |
GRCh38 GRCh38 GRCh37 |
68 | 205 | |
BHLHA9 | - | - |
GRCh38 GRCh37 |
53 | 177 | |
CRK | - | - |
GRCh38 GRCh38 GRCh37 |
9 | 121 | |
DOC2B | - | - |
GRCh38 GRCh38 GRCh37 |
14 | 67 | |
DPH1 | - | - |
GRCh38 GRCh37 |
82 | 174 | |
GEMIN4 | - | - |
GRCh38 GRCh37 |
147 | 253 | |
GLOD4 | - | - | - |
GRCh38 GRCh37 |
15 | 124 |
There are 33 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 |
---|---|---|---|---|
Uncertain significance (1) |
|
Apr 1, 2018 | RCV000754117.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023