ClinVar Miner

List of variants in gene CYP19A1, MIR4713HG, PIRC66 studied for 46,XX disorder of sex development

Included ClinVar conditions (32):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 51
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HGVS dbSNP
NM_031226.2(CYP19A1):c.*1019C>T rs886051274
NM_031226.2(CYP19A1):c.*1069C>T rs527275486
NM_031226.2(CYP19A1):c.*108A>G rs28757207
NM_031226.2(CYP19A1):c.*1296T>C rs28757212
NM_031226.2(CYP19A1):c.*1601G>A rs12148604
NM_031226.2(CYP19A1):c.*1608C>T rs781782351
NM_031226.2(CYP19A1):c.*161T>G rs4646
NM_031226.2(CYP19A1):c.*166T>A rs181721810
NM_031226.2(CYP19A1):c.*1877T>G rs886051273
NM_031226.2(CYP19A1):c.*1888A>G rs4275794
NM_031226.2(CYP19A1):c.*191C>A rs190403648
NM_031226.2(CYP19A1):c.*191delC rs546415613
NM_031226.2(CYP19A1):c.*19C>T rs10046
NM_031226.2(CYP19A1):c.*2032G>A rs886051272
NM_031226.2(CYP19A1):c.*2039G>T rs35636804
NM_031226.2(CYP19A1):c.*2155T>C rs865821138
NM_031226.2(CYP19A1):c.*2170G>A rs2255192
NM_031226.2(CYP19A1):c.*2192T>C rs886051271
NM_031226.2(CYP19A1):c.*2257A>G rs540900346
NM_031226.2(CYP19A1):c.*2258_*2259insA rs3217422
NM_031226.2(CYP19A1):c.*2274A>G rs886051270
NM_031226.2(CYP19A1):c.*2467G>A rs934634
NM_031226.2(CYP19A1):c.*2511G>A rs934633
NM_031226.2(CYP19A1):c.*2645dupC rs886051269
NM_031226.2(CYP19A1):c.*280A>T rs77828415
NM_031226.2(CYP19A1):c.*460G>C rs28757208
NM_031226.2(CYP19A1):c.*483G>C rs886051276
NM_031226.2(CYP19A1):c.*638G>T rs886051275
NM_031226.2(CYP19A1):c.*747G>A rs866111735
NM_031226.2(CYP19A1):c.*858C>T rs555261840
NM_031226.2(CYP19A1):c.*9G>T rs373757519
NM_031226.2(CYP19A1):c.1094G>A (p.Arg365Gln) rs80051519
NM_031226.2(CYP19A1):c.1123C>T (p.Arg375Cys) rs121434536
NM_031226.2(CYP19A1):c.115T>C (p.Trp39Arg) rs2236722
NM_031226.2(CYP19A1):c.1224del (p.Lys409Asnfs) rs786205108
NM_031226.2(CYP19A1):c.1303C>T (p.Arg435Cys) rs121434534
NM_031226.2(CYP19A1):c.1310G>A (p.Cys437Tyr) rs78310315
NM_031226.2(CYP19A1):c.1378G>A (p.Val460Met) rs372500474
NM_031226.2(CYP19A1):c.186C>T (p.His62=) rs60308277
NM_031226.2(CYP19A1):c.240A>G (p.Val80=) rs700518
NM_031226.2(CYP19A1):c.296+1G>A rs786205109
NM_031226.2(CYP19A1):c.49G>A (p.Val17Met) rs200111039
NM_031226.2(CYP19A1):c.602C>T (p.Thr201Met) rs28757184
NM_031226.2(CYP19A1):c.628G>A (p.Glu210Lys) rs121434538
NM_031226.2(CYP19A1):c.629-10T>C rs781489846
NM_031226.2(CYP19A1):c.629-3C>A rs786205110
NM_031226.2(CYP19A1):c.629-8dupT rs750758078
NM_031226.2(CYP19A1):c.743+2T>C rs786205107
NM_031226.2(CYP19A1):c.790C>T (p.Arg264Cys) rs700519
NM_031226.2(CYP19A1):c.953T>C (p.Met318Thr) rs143839949
NM_031226.2(CYP19A1):c.976C>T (p.Pro326Ser) rs368902124

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