ClinVar Genomic variation as it relates to human health
GRCh37/hg19 19p13.11-11(chr19:16526787-24631604)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 | |||
PIK3R2 | No evidence available | No evidence available |
GRCh38 GRCh37 |
354 | 428 | |
ABHD8 | - | - | - |
GRCh38 GRCh37 |
- | 36 |
ANKLE1 | - | - |
GRCh38 GRCh37 |
75 | 93 | |
ANO8 | - | - |
GRCh38 GRCh37 |
78 | 105 | |
ARMC6 | - | - | - |
GRCh38 GRCh37 |
32 | 42 |
ARRDC2 | - | - | - |
GRCh38 GRCh37 |
24 | 38 |
ATP13A1 | - | - |
GRCh38 GRCh37 |
81 | 109 | |
B3GNT3 | - | - |
GRCh38 GRCh37 |
24 | 34 | |
BABAM1 | - | - |
GRCh38 GRCh37 |
15 | 32 | |
BORCS8 | - | - |
GRCh38 GRCh37 |
- | 29 |
There are 122 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 |
---|---|---|---|---|
Pathogenic (1) |
|
Jun 5, 2012 | RCV000752593.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 06, 2024