ClinVar Miner

List of variants in gene combination CYP19A1, MIR4713HG, PIRC66 reported as uncertain significance for female infertility

Included ClinVar conditions (89):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 75
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HGVS dbSNP gnomAD frequency
NM_000103.4(CYP19A1):c.*1889A>T rs762427390 0.00067
NM_000103.4(CYP19A1):c.*2257A>G rs540900346 0.00067
NM_000103.4(CYP19A1):c.49G>A (p.Val17Met) rs200111039 0.00030
NM_000103.4(CYP19A1):c.*1069C>T rs527275486 0.00028
NM_000103.4(CYP19A1):c.*125T>C rs781742620 0.00024
NM_000103.4(CYP19A1):c.*2536C>T rs140417660 0.00023
NM_000103.4(CYP19A1):c.*2155T>C rs865821138 0.00019
NM_000103.4(CYP19A1):c.*2274A>G rs886051270 0.00019
NM_000103.4(CYP19A1):c.*1608C>T rs781782351 0.00018
NM_000103.4(CYP19A1):c.953T>C (p.Met318Thr) rs143839949 0.00017
NM_000103.4(CYP19A1):c.*858C>T rs555261840 0.00016
NM_000103.4(CYP19A1):c.721T>A (p.Tyr241Asn) rs143562020 0.00016
NM_000103.4(CYP19A1):c.465C>T (p.Pro155=) rs146495071 0.00012
NM_000103.4(CYP19A1):c.467G>A (p.Gly156Asp) rs142652579 0.00009
NM_000103.4(CYP19A1):c.*166T>A rs181721810 0.00006
NM_000103.4(CYP19A1):c.*9G>T rs373757519 0.00006
NM_000103.4(CYP19A1):c.1353C>T (p.Leu451=) rs774940170 0.00006
NM_000103.4(CYP19A1):c.336C>T (p.Tyr112=) rs139905959 0.00006
NM_000103.4(CYP19A1):c.*747G>A rs866111735 0.00005
NM_000103.4(CYP19A1):c.*2519T>C rs1234949259 0.00004
NM_000103.4(CYP19A1):c.1387T>C (p.Leu463=) rs377327265 0.00004
NM_000103.4(CYP19A1):c.1488C>T (p.Asn496=) rs374079882 0.00004
NM_000103.4(CYP19A1):c.99C>A (p.Gly33=) rs779177368 0.00004
NM_000103.4(CYP19A1):c.*2032G>A rs886051272 0.00003
NM_000103.4(CYP19A1):c.242A>G (p.Tyr81Cys) rs199845027 0.00003
NM_000103.4(CYP19A1):c.629-10T>C rs781489846 0.00003
NM_000103.4(CYP19A1):c.*2086G>A rs989880661 0.00002
NM_000103.4(CYP19A1):c.*2497T>C rs752484173 0.00002
NM_000103.4(CYP19A1):c.1113C>T (p.Asp371=) rs774007712 0.00002
NM_000103.4(CYP19A1):c.1221C>T (p.Phe407=) rs764767709 0.00002
NM_000103.4(CYP19A1):c.1263+8C>A rs757404619 0.00002
NM_000103.4(CYP19A1):c.237G>A (p.Arg79=) rs749406233 0.00002
NM_000103.4(CYP19A1):c.859-6G>T rs756838912 0.00002
NM_000103.4(CYP19A1):c.*1019C>T rs886051274 0.00001
NM_000103.4(CYP19A1):c.*1381C>T rs1047960680 0.00001
NM_000103.4(CYP19A1):c.*1877T>G rs886051273 0.00001
NM_000103.4(CYP19A1):c.*2126G>A rs977456146 0.00001
NM_000103.4(CYP19A1):c.1230C>T (p.Pro410=) rs775991900 0.00001
NM_000103.4(CYP19A1):c.1425C>T (p.His475=) rs982752444 0.00001
NM_000103.4(CYP19A1):c.146-7G>T rs1262602894 0.00001
NM_000103.4(CYP19A1):c.501C>A (p.Ser167=) rs35900050 0.00001
NM_000103.4(CYP19A1):c.625G>A (p.Asp209Asn) rs748459967 0.00001
NM_000103.4(CYP19A1):c.637A>G (p.Ile213Val) rs1045354487 0.00001
NM_000103.4(CYP19A1):c.907A>G (p.Met303Val) rs2031445857 0.00001
NM_000103.4(CYP19A1):c.*1364C>T rs2030715622
NM_000103.4(CYP19A1):c.*1441G>A rs943520982
NM_000103.4(CYP19A1):c.*1545G>T rs2030691135
NM_000103.4(CYP19A1):c.*1833C>A rs2030664773
NM_000103.4(CYP19A1):c.*1878T>C rs2030660970
NM_000103.4(CYP19A1):c.*1888A>T rs4275794
NM_000103.4(CYP19A1):c.*191C>A rs190403648
NM_000103.4(CYP19A1):c.*191del rs546415613
NM_000103.4(CYP19A1):c.*2067T>G rs1042269504
NM_000103.4(CYP19A1):c.*2192T>C rs886051271
NM_000103.4(CYP19A1):c.*240C>A rs1379933476
NM_000103.4(CYP19A1):c.*2589C>A rs751474218
NM_000103.4(CYP19A1):c.*2607A>G rs878905692
NM_000103.4(CYP19A1):c.*2645dup rs886051269
NM_000103.4(CYP19A1):c.*483G>C rs886051276
NM_000103.4(CYP19A1):c.*638G>T rs886051275
NM_000103.4(CYP19A1):c.*646C>G rs2030790688
NM_000103.4(CYP19A1):c.*78G>T rs28757206
NM_000103.4(CYP19A1):c.1133T>C (p.Leu378Ser) rs2031101006
NM_000103.4(CYP19A1):c.1212C>A (p.Leu404=) rs772086882
NM_000103.4(CYP19A1):c.1378G>A (p.Val460Met) rs372500474
NM_000103.4(CYP19A1):c.138A>C (p.Ser46=) rs766042143
NM_000103.4(CYP19A1):c.196C>T (p.Leu66=) rs2033435368
NM_000103.4(CYP19A1):c.228C>T (p.Tyr76=) rs775978298
NM_000103.4(CYP19A1):c.357A>C (p.Lys119Asn) rs2032722258
NM_000103.4(CYP19A1):c.493G>A (p.Ala165Thr) rs769769335
NM_000103.4(CYP19A1):c.538A>G (p.Asn180Asp)
NM_000103.4(CYP19A1):c.629-8dup rs750758078
NM_000103.4(CYP19A1):c.859-9A>G
NM_000103.4(CYP19A1):c.924T>G (p.Pro308=) rs371448768
NM_000103.4(CYP19A1):c.953T>A (p.Met318Lys)

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