ClinVar Genomic variation as it relates to human health
GRCh38/hg38 17p13.3(chr17:847955-1641601)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 | |||
ABR | No evidence available | No evidence available |
GRCh38 GRCh38 GRCh38 GRCh37 |
54 | 183 | |
PITPNA | No evidence available | No evidence available |
GRCh38 GRCh37 |
8 | 114 | |
YWHAE | No evidence available | No evidence available |
GRCh38 GRCh38 GRCh37 |
69 | 209 | |
ABR-AS1 | - | - | - |
GRCh38 GRCh38 |
- | 38 |
BHLHA9 | - | - |
GRCh38 GRCh37 |
60 | 187 | |
CRK | - | - |
GRCh38 GRCh38 GRCh37 |
15 | 130 | |
INPP5K | - | - |
GRCh38 GRCh37 |
100 | 210 | |
LOC101927727 | - | - | - | GRCh38 | - | 33 |
LOC112529892 | - | - | - |
GRCh38 GRCh38 |
- | 48 |
LOC121587569 | - | - | - |
GRCh38 GRCh38 GRCh38 |
- | 32 |
There are 35 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 |
---|---|---|---|---|
See cases
|
Pathogenic (1) |
|
Jan 24, 2011 | RCV000135574.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024