ClinVar Genomic variation as it relates to human health
GRCh37/hg19 Yq11.21-11.221(chrY:14443478-15230544)x0
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 | |||
DDX3Y | - | - |
GRCh38 GRCh37 |
5 | 75 | |
TTTY15 | - | - | - |
GRCh38 GRCh37 |
1 | 72 |
USP9Y | - | - |
GRCh38 GRCh37 |
17 | 92 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Pathogenic (1) |
|
Dec 3, 2019 | RCV001090082.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022