ClinVar Miner

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

Included ClinVar conditions (7):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
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NM_000103.4(CYP19A1):c.*1296T>C rs28757212
NM_000103.4(CYP19A1):c.*2039G>T rs35636804
NM_000103.4(CYP19A1):c.*2511G>A rs934633
NM_000103.4(CYP19A1):c.*280A>T rs77828415
NM_000103.4(CYP19A1):c.115T>C (p.Trp39Arg) rs2236722
NM_000103.4(CYP19A1):c.186C>T (p.His62=) rs60308277
NM_000103.4(CYP19A1):c.602C>T (p.Thr201Met) rs28757184
NM_000103.4(CYP19A1):c.790C>T (p.Arg264Cys) rs700519

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