Annotation Detail
Information
- Associated Genes
- AMELY RBMY1A1 RPS4Y1 SRY TSPY1 UTY ZFY KDM5D USP9Y DDX3Y VCY EIF1AY TMSB4Y CDY2A NLGN4Y TTTY1 TTTY2 TSPY2 TTTY15 PCDH11Y TTTY9A TTTY11 TTTY12 TTTY13 TTTY14 TTTY8 HSFY1 TGIF2LY TBL1Y RPS4Y2 HSFY2 TTTY10 TTTY7 TTTY16 TTTY18 TTTY20 TTTY19 TTTY21 TTTY22 TTTY23 VCY1B RBMY1B RBMY1D RBMY1E TTTY9B TSPY3 TSPY4 TSPY8 TTTY21B TTTY1B TTTY2B TTTY8B TTTY7B TTTY23B FAM197Y9 TTTY13B FAM197Y10 TSPY10 FAM197Y1 PRORY
- Associated Variants
- GRCh37/hg19 Yp11.31-q11.223(chrY:2650140-24070172)x2
- Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- GRCh37/hg19 Yp11.31-q11.223(chrY:2650140-24070172)x2 AND not provided
- ClinVar Allele ID
- 556153
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2017-10-25
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000684444
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs