ClinVar Miner

List of variants studied for 46,XX disorder of sex development induced by fetoplacental androgens excess

Included ClinVar conditions (1):
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Total variants: 100
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HGVS dbSNP
CYP19A1, 1-BP DEL, C, CODON 156
NM_000103.4(CYP19A1):c.*1019C>T rs886051274
NM_000103.4(CYP19A1):c.*1069C>T rs527275486
NM_000103.4(CYP19A1):c.*108A>G rs28757207
NM_000103.4(CYP19A1):c.*1190C>T
NM_000103.4(CYP19A1):c.*125T>C
NM_000103.4(CYP19A1):c.*1296T>C rs28757212
NM_000103.4(CYP19A1):c.*1364C>T
NM_000103.4(CYP19A1):c.*1381C>T
NM_000103.4(CYP19A1):c.*1441G>A
NM_000103.4(CYP19A1):c.*1545G>T
NM_000103.4(CYP19A1):c.*1601G>A rs12148604
NM_000103.4(CYP19A1):c.*1608C>T rs781782351
NM_000103.4(CYP19A1):c.*161T>G rs4646
NM_000103.4(CYP19A1):c.*166T>A rs181721810
NM_000103.4(CYP19A1):c.*1833C>A
NM_000103.4(CYP19A1):c.*1877T>G rs886051273
NM_000103.4(CYP19A1):c.*1878T>C
NM_000103.4(CYP19A1):c.*1888A>G rs4275794
NM_000103.4(CYP19A1):c.*1888A>T
NM_000103.4(CYP19A1):c.*1889A>T
NM_000103.4(CYP19A1):c.*191C>A rs190403648
NM_000103.4(CYP19A1):c.*191del rs546415613
NM_000103.4(CYP19A1):c.*19C>T rs10046
NM_000103.4(CYP19A1):c.*2032G>A rs886051272
NM_000103.4(CYP19A1):c.*2039G>T rs35636804
NM_000103.4(CYP19A1):c.*2067T>G
NM_000103.4(CYP19A1):c.*2086G>A
NM_000103.4(CYP19A1):c.*2126G>A
NM_000103.4(CYP19A1):c.*2155T>C rs865821138
NM_000103.4(CYP19A1):c.*2170G>A rs2255192
NM_000103.4(CYP19A1):c.*2192T>C rs886051271
NM_000103.4(CYP19A1):c.*2257A>G rs540900346
NM_000103.4(CYP19A1):c.*2258_*2259insA rs3217422
NM_000103.4(CYP19A1):c.*2274A>G rs886051270
NM_000103.4(CYP19A1):c.*240C>A
NM_000103.4(CYP19A1):c.*2467G>A rs934634
NM_000103.4(CYP19A1):c.*2497T>C
NM_000103.4(CYP19A1):c.*2511G>A rs934633
NM_000103.4(CYP19A1):c.*2519T>C
NM_000103.4(CYP19A1):c.*2536C>T
NM_000103.4(CYP19A1):c.*2589C>A
NM_000103.4(CYP19A1):c.*2607A>G
NM_000103.4(CYP19A1):c.*2624C>T
NM_000103.4(CYP19A1):c.*2632T>C
NM_000103.4(CYP19A1):c.*2645dup rs886051269
NM_000103.4(CYP19A1):c.*2723A>G
NM_000103.4(CYP19A1):c.*280A>T rs77828415
NM_000103.4(CYP19A1):c.*460G>C rs28757208
NM_000103.4(CYP19A1):c.*483G>C rs886051276
NM_000103.4(CYP19A1):c.*53C>T
NM_000103.4(CYP19A1):c.*543C>G
NM_000103.4(CYP19A1):c.*638G>T rs886051275
NM_000103.4(CYP19A1):c.*646C>G
NM_000103.4(CYP19A1):c.*747G>A rs866111735
NM_000103.4(CYP19A1):c.*78G>T
NM_000103.4(CYP19A1):c.*858C>T rs555261840
NM_000103.4(CYP19A1):c.*9G>T rs373757519
NM_000103.4(CYP19A1):c.-118G>A
NM_000103.4(CYP19A1):c.-39+14572C>T rs530192973
NM_000103.4(CYP19A1):c.-39+14624_-39+14625del rs780146461
NM_000103.4(CYP19A1):c.-39+14640A>G
NM_000103.4(CYP19A1):c.-39+14646C>T
NM_000103.4(CYP19A1):c.-39+14659C>A rs28757082
NM_000103.4(CYP19A1):c.-39+1G>A rs956997586
NM_000103.4(CYP19A1):c.1094G>A (p.Arg365Gln) rs80051519
NM_000103.4(CYP19A1):c.109T>C (p.Leu37=) rs58282176
NM_000103.4(CYP19A1):c.1123C>T (p.Arg375Cys) rs121434536
NM_000103.4(CYP19A1):c.115T>C (p.Trp39Arg) rs2236722
NM_000103.4(CYP19A1):c.1224C>T (p.Pro408=)
NM_000103.4(CYP19A1):c.1224del (p.Lys409fs) rs786205108
NM_000103.4(CYP19A1):c.1230C>T (p.Pro410=)
NM_000103.4(CYP19A1):c.1303C>T (p.Arg435Cys) rs121434534
NM_000103.4(CYP19A1):c.1310G>A (p.Cys437Tyr) rs78310315
NM_000103.4(CYP19A1):c.1378G>A (p.Val460Met) rs372500474
NM_000103.4(CYP19A1):c.1488C>T (p.Asn496=)
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.242A>G (p.Tyr81Cys)
NM_000103.4(CYP19A1):c.24G>A (p.Pro8=)
NM_000103.4(CYP19A1):c.296+1G>A rs786205109
NM_000103.4(CYP19A1):c.336C>T (p.Tyr112=)
NM_000103.4(CYP19A1):c.357A>C (p.Lys119Asn)
NM_000103.4(CYP19A1):c.383A>G (p.His128Arg)
NM_000103.4(CYP19A1):c.42C>G (p.Thr14=) rs61203654
NM_000103.4(CYP19A1):c.465C>T (p.Pro155=)
NM_000103.4(CYP19A1):c.49G>A (p.Val17Met) rs200111039
NM_000103.4(CYP19A1):c.501C>A (p.Ser167=)
NM_000103.4(CYP19A1):c.602C>T (p.Thr201Met) rs28757184
NM_000103.4(CYP19A1):c.628G>A (p.Glu210Lys) rs121434538
NM_000103.4(CYP19A1):c.629-10T>C rs781489846
NM_000103.4(CYP19A1):c.629-16dup rs750758078
NM_000103.4(CYP19A1):c.629-3C>A rs786205110
NM_000103.4(CYP19A1):c.721T>A (p.Tyr241Asn)
NM_000103.4(CYP19A1):c.743+2T>C rs786205107
NM_000103.4(CYP19A1):c.790C>T (p.Arg264Cys) rs700519
NM_000103.4(CYP19A1):c.924T>G (p.Pro308=)
NM_000103.4(CYP19A1):c.953T>C (p.Met318Thr) rs143839949
NM_000103.4(CYP19A1):c.963C>G (p.Leu321=)
NM_000103.4(CYP19A1):c.976C>T (p.Pro326Ser) rs368902124

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