ClinVar Miner

List of variants in gene combination CYP19A1, MIR4713HG, PIRC66 reported as benign for 46,XX disorder of sex development induced by fetoplacental androgens excess

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
Download table as spreadsheet
NM_000103.4(CYP19A1):c.*108A>G rs28757207
NM_000103.4(CYP19A1):c.*1296T>C rs28757212
NM_000103.4(CYP19A1):c.*1601G>A rs12148604
NM_000103.4(CYP19A1):c.*161T>G rs4646
NM_000103.4(CYP19A1):c.*1888A>G rs4275794
NM_000103.4(CYP19A1):c.*19C>T rs10046
NM_000103.4(CYP19A1):c.*2039G>T rs35636804
NM_000103.4(CYP19A1):c.*2170G>A rs2255192
NM_000103.4(CYP19A1):c.*2258_*2259insA rs3217422
NM_000103.4(CYP19A1):c.*2467G>A rs934634
NM_000103.4(CYP19A1):c.*2511G>A rs934633
NM_000103.4(CYP19A1):c.*280A>T rs77828415
NM_000103.4(CYP19A1):c.109T>C (p.Leu37=) rs58282176
NM_000103.4(CYP19A1):c.1224C>T (p.Pro408=) rs2304461
NM_000103.4(CYP19A1):c.186C>T (p.His62=) rs60308277
NM_000103.4(CYP19A1):c.240A>G (p.Val80=) rs700518
NM_000103.4(CYP19A1):c.602C>T (p.Thr201Met) rs28757184
NM_000103.4(CYP19A1):c.790C>T (p.Arg264Cys) rs700519
NM_000103.4(CYP19A1):c.963C>G (p.Leu321=) rs59359360

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.