ClinVar Miner

List of variants in gene combination CYP19A1, MIR4713HG, PIRC66 reported as benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 52
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000103.4(CYP19A1):c.*161T>G rs4646 0.70442
NM_000103.4(CYP19A1):c.858+118A>C rs2289106 0.50678
NM_000103.4(CYP19A1):c.1022-53T>G rs1065779 0.49578
NM_000103.4(CYP19A1):c.*1601G>A rs12148604 0.46111
NM_000103.4(CYP19A1):c.*2258_*2259insA rs3217422 0.45798
NM_000103.4(CYP19A1):c.1022-176A>C rs8029120 0.43150
NM_000103.4(CYP19A1):c.*19C>T rs10046 0.42803
NM_000103.4(CYP19A1):c.744-106T>G rs2304463 0.42478
NM_000103.4(CYP19A1):c.859-79A>G rs2289105 0.42460
NM_000103.4(CYP19A1):c.629-16T>G rs4324076 0.42328
NM_000103.4(CYP19A1):c.743+36A>T rs1143704 0.42261
NM_000103.4(CYP19A1):c.146-59A>G rs3759811 0.39773
NM_000103.4(CYP19A1):c.297-76A>G rs1065778 0.39712
NM_000103.4(CYP19A1):c.240A>G (p.Val80=) rs700518 0.39685
NM_000103.4(CYP19A1):c.-38-12791G>C rs1062033 0.34972
NM_000103.4(CYP19A1):c.*2170G>A rs2255192 0.24313
NM_000103.4(CYP19A1):c.*2467G>A rs934634 0.23844
NM_000103.4(CYP19A1):c.*1888A>G rs4275794 0.16667
NM_000103.4(CYP19A1):c.858+106A>G rs2289107 0.12651
NM_000103.4(CYP19A1):c.*2511G>A rs934633 0.09620
NM_000103.4(CYP19A1):c.858+26C>T rs17601241 0.08462
NM_000103.4(CYP19A1):c.790C>T (p.Arg264Cys) rs700519 0.08141
NM_000103.4(CYP19A1):c.859-181G>A rs28757192 0.03860
NM_000103.4(CYP19A1):c.602C>T (p.Thr201Met) rs28757184 0.03608
NM_000103.4(CYP19A1):c.*2039G>T rs35636804 0.03278
NM_000103.4(CYP19A1):c.186C>T (p.His62=) rs60308277 0.02885
NM_000103.4(CYP19A1):c.*1296T>C rs28757212 0.02370
NM_000103.4(CYP19A1):c.1264-225G>A rs28757205 0.01903
NM_000103.4(CYP19A1):c.146-27T>C rs28377729 0.01793
NM_000103.4(CYP19A1):c.*1190C>T rs28757210 0.00584
NM_000103.4(CYP19A1):c.109T>C (p.Leu37=) rs58282176 0.00583
NM_000103.4(CYP19A1):c.*2723A>G rs2289104 0.00409
NM_000103.4(CYP19A1):c.*280A>T rs77828415 0.00341
NM_000103.4(CYP19A1):c.963C>G (p.Leu321=) rs59359360 0.00160
NM_000103.4(CYP19A1):c.115T>C (p.Trp39Arg) rs2236722 0.00129
NM_000103.4(CYP19A1):c.451+8G>A rs28892004 0.00118
NM_000103.4(CYP19A1):c.475C>T (p.Arg159Cys) rs201842322 0.00047
NM_000103.4(CYP19A1):c.*108A>G rs28757207 0.00019
NM_000103.4(CYP19A1):c.75C>T (p.Thr25=) rs745979108 0.00010
NM_000103.4(CYP19A1):c.1224C>T (p.Pro408=) rs2304461 0.00009
NM_000103.4(CYP19A1):c.242A>G (p.Tyr81Cys) rs199845027 0.00003
NM_000103.4(CYP19A1):c.*2624C>T rs562193184 0.00002
NM_000103.4(CYP19A1):c.1264-6del rs2542388984
NM_000103.4(CYP19A1):c.1370G>A (p.Arg457Gln) rs770120065
NM_000103.4(CYP19A1):c.451+28_451+29insCTT rs386382978
NM_000103.4(CYP19A1):c.451+28_451+30dup rs11575899
NM_000103.4(CYP19A1):c.451+79TATT[11] rs57921193
NM_000103.4(CYP19A1):c.451+79TATT[8] rs57921193
NM_000103.4(CYP19A1):c.603G>T (p.Thr201=) rs774856159
NM_000103.4(CYP19A1):c.629-8del rs750758078
NM_000103.4(CYP19A1):c.629-8dup rs750758078
NM_000103.4(CYP19A1):c.744-5del rs753996652

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.