ClinVar Miner

List of variants in gene YY1 reported as uncertain significance by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_003403.5(YY1):c.1003G>A (p.Val335Ile)
NM_003403.5(YY1):c.1062G>C (p.Gln354His)
NM_003403.5(YY1):c.1082G>A (p.Gly361Glu)
NM_003403.5(YY1):c.1100A>C (p.Asp367Ala)
NM_003403.5(YY1):c.167_172del (p.Gly56_Gly57del) rs2549127188
NM_003403.5(YY1):c.178G>A (p.Gly60Ser)
NM_003403.5(YY1):c.233A>G (p.His78Arg)
NM_003403.5(YY1):c.281C>T (p.Pro94Leu) rs1890691522
NM_003403.5(YY1):c.288_299del (p.Gln96_His99del)
NM_003403.5(YY1):c.293A>G (p.His98Arg) rs2549127314
NM_003403.5(YY1):c.31A>T (p.Thr11Ser) rs1271244582
NM_003403.5(YY1):c.323C>G (p.Thr108Arg)
NM_003403.5(YY1):c.488G>C (p.Gly163Ala)
NM_003403.5(YY1):c.635_640del (p.Ile212_Lys213del)
NM_003403.5(YY1):c.685_690del (p.Lys229_Lys230del)
NM_003403.5(YY1):c.73G>A (p.Glu25Lys) rs2549127119
NM_003403.5(YY1):c.742C>T (p.Pro248Ser) rs2139589755
NM_003403.5(YY1):c.893G>A (p.Cys298Tyr)
NM_003403.5(YY1):c.952C>T (p.His318Tyr) rs1891320903

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.