ClinVar Genomic variation as it relates to human health
GRCh37/hg19 16p12.2-11.2(chr16:21576803-30177240)x3
Germline
Classification
(1)
Pathogenic
criteria provided, single submitter
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 | |||
PRRT2 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
6 | 896 | |
SH2B1 | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
211 | 367 | |
ALDOA | - | - |
GRCh38 GRCh37 |
1 | 560 | |
APOBR | - | - |
GRCh38 GRCh37 |
43 | 131 | |
AQP8 | - | - |
GRCh38 GRCh37 |
25 | 57 | |
ARHGAP17 | - | - |
GRCh38 GRCh38 GRCh37 |
48 | 80 | |
ASPHD1 | - | - | - |
GRCh38 GRCh37 |
20 | 313 |
ATP2A1 | - | - |
GRCh38 GRCh37 |
770 | 969 | |
ATXN2L | - | - |
GRCh38 GRCh37 |
46 | 204 | |
BOLA2 | - | - |
GRCh38 GRCh37 |
- | 87 |
There are 85 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 8, 2022 | RCV002474541.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 26, 2023