ClinVar Genomic variation as it relates to human health
GRCh37/hg19 Yq11.223-12(chrY:26137299-59336737)x0
Germline
Classification
(1)
Likely 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 | |||
CDY1 | No evidence available | No evidence available |
GRCh38 GRCh37 |
- | 94 | |
BPY2B | - | - | - |
GRCh38 GRCh37 |
- | 102 |
BPY2C | - | - | - |
GRCh38 GRCh37 |
- | 100 |
DAZ3 | - | - |
GRCh38 GRCh37 |
- | 102 | |
DAZ4 | - | - |
GRCh38 GRCh37 |
- | 103 | |
TTTY17B | - | - | - |
GRCh38 GRCh37 |
- | 102 |
TTTY17C | - | - | - |
GRCh38 GRCh37 |
- | 98 |
TTTY3 | - | - |
GRCh38 GRCh37 |
- | 91 | |
TTTY4B | - | - | - |
GRCh38 GRCh37 |
- | 102 |
TTTY4C | - | - | - |
GRCh38 GRCh37 |
- | 100 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Likely pathogenic (1) |
|
Jan 12, 2015 | RCV000512115.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024