ClinVar Genomic variation as it relates to human health
GRCh37/hg19 15q11.2-12(chr15:24740574-25955228)x1
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 | |||
UBE3A | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
34 | 1202 | |
SNURF | - | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
- | 364 |
ATP10A | No evidence available | No evidence available |
GRCh38 GRCh37 |
180 | 486 | |
SNRPN | No evidence available | No evidence available |
GRCh38 GRCh37 |
3 | 393 | |
IPW | - | - |
GRCh38 GRCh37 |
- | 305 | |
NPAP1 | - | - |
GRCh38 GRCh37 |
92 | 408 | |
PWAR1 | - | - |
GRCh38 GRCh37 |
- | 306 | |
PWAR4 | - | - | - |
GRCh38 GRCh37 |
- | 305 |
PWAR5 | - | - |
GRCh38 GRCh37 |
- | 307 | |
PWAR6 | - | - | - |
GRCh38 GRCh37 |
- | 306 |
There are 4 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) |
|
- | RCV003987105.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 30, 2024