ClinVar Genomic variation as it relates to human health
GRCh38/hg38 17p13.3-13.2(chr17:1348488-3513273)x3
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 | |||
PAFAH1B1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
521 | 604 | |
PITPNA | No evidence available | No evidence available |
GRCh38 GRCh37 |
6 | 109 | |
YWHAE | No evidence available | No evidence available |
GRCh38 GRCh38 GRCh37 |
69 | 206 | |
ASPA | - | - |
GRCh38 GRCh37 |
13 | 475 | |
CCDC92B | - | - | - | GRCh38 | - | 25 |
CLUH | - | - |
GRCh38 GRCh37 |
92 | 161 | |
CRK | - | - |
GRCh38 GRCh38 GRCh37 |
12 | 124 | |
DPH1 | - | - |
GRCh38 GRCh37 |
94 | 190 | |
HIC1 | - | - |
GRCh38 GRCh37 |
19 | 117 | |
INPP5K | - | - |
GRCh38 GRCh37 |
95 | 202 |
There are 166 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) |
|
Jun 14, 2011 | RCV000137603.7 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024