ClinVar Miner

List of variants in gene NR3C1 reported as uncertain significance for adrenogenital syndrome

Included ClinVar conditions (12):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 96
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HGVS dbSNP gnomAD frequency
NM_000176.3(NR3C1):c.*3877C>T rs10482716 0.00291
NM_000176.3(NR3C1):c.685G>A (p.Ala229Thr) rs72542742 0.00134
NM_000176.3(NR3C1):c.*2056dup rs886060046 0.00076
NM_000176.3(NR3C1):c.*808T>C rs182544753 0.00075
NM_000176.3(NR3C1):c.*1176C>T rs61753504 0.00072
NM_000176.3(NR3C1):c.*3330G>T rs61753512 0.00072
NM_000176.3(NR3C1):c.*3937A>T rs4518436 0.00066
NM_000176.3(NR3C1):c.*3580T>C rs61754801 0.00059
NM_000176.3(NR3C1):c.*954C>G rs766219976 0.00055
NM_000176.3(NR3C1):c.*1628A>G rs372713535 0.00038
NM_001018077.1(NR3C1):c.-553G>A rs536482885 0.00038
NM_000176.3(NR3C1):c.*1464A>G rs572503540 0.00035
NM_000176.3(NR3C1):c.*3300G>T rs72542770 0.00035
NM_000176.3(NR3C1):c.*937C>A rs72542760 0.00031
NM_000176.3(NR3C1):c.*3003A>G rs61753509 0.00027
NM_001018077.1(NR3C1):c.-367G>A rs531630337 0.00025
NM_000176.3(NR3C1):c.*3406C>G rs771678306 0.00023
NM_000176.3(NR3C1):c.*2956G>A rs535011433 0.00015
NM_000176.3(NR3C1):c.88T>C (p.Tyr30His) rs143711342 0.00014
NM_000176.3(NR3C1):c.*2928A>G rs763603358 0.00013
NM_000176.3(NR3C1):c.*3383T>G rs983670372 0.00011
NM_001018077.1(NR3C1):c.-464G>T rs372764988 0.00011
NM_000176.3(NR3C1):c.*256A>G rs13306585 0.00009
NM_000176.3(NR3C1):c.753G>A (p.Pro251=) rs375379753 0.00008
NM_000176.3(NR3C1):c.*1825G>C rs1035379863 0.00006
NM_000176.3(NR3C1):c.*3319G>C rs886060039 0.00006
NM_000176.3(NR3C1):c.*618A>G rs886060056 0.00006
NM_000176.3(NR3C1):c.*905A>T rs1034700180 0.00006
NM_000176.3(NR3C1):c.631A>G (p.Ser211Gly) rs886060061 0.00006
NM_000176.3(NR3C1):c.*1509C>A rs886060048 0.00003
NM_000176.3(NR3C1):c.*1957A>G rs968998036 0.00003
NM_000176.3(NR3C1):c.*36G>A rs761674033 0.00003
NM_000176.3(NR3C1):c.*3868C>T rs941331534 0.00003
NM_000176.3(NR3C1):c.*2875T>C rs1421087791 0.00002
NM_000176.3(NR3C1):c.*293A>C rs1396658562 0.00002
NM_000176.3(NR3C1):c.*3466T>C rs886060037 0.00002
NM_000176.3(NR3C1):c.*1466T>C rs1812917346 0.00001
NM_000176.3(NR3C1):c.*1941A>C rs1239987236 0.00001
NM_000176.3(NR3C1):c.*2367C>T rs568718223 0.00001
NM_000176.3(NR3C1):c.*2370G>A rs753145816 0.00001
NM_000176.3(NR3C1):c.*2567A>G rs886060044 0.00001
NM_000176.3(NR3C1):c.*2873G>A rs886060042 0.00001
NM_000176.3(NR3C1):c.*3046G>C rs886060041 0.00001
NM_000176.3(NR3C1):c.*3685C>G rs10482715 0.00001
NM_000176.3(NR3C1):c.*3846G>A rs1365619187 0.00001
NM_000176.3(NR3C1):c.*752A>G rs869125609 0.00001
NM_000176.3(NR3C1):c.*988T>C rs773208301 0.00001
NM_000176.3(NR3C1):c.1039C>G (p.Gln347Glu) rs148470701 0.00001
NM_000176.3(NR3C1):c.2309A>G (p.Lys770Arg) rs751136795 0.00001
NM_000176.3(NR3C1):c.309A>T (p.Gly103=) rs779300133 0.00001
NM_000176.3(NR3C1):c.850A>G (p.Ile284Val) rs766200119 0.00001
NM_001018077.1(NR3C1):c.-531G>A rs1462093593 0.00001
NM_000176.3(NR3C1):c.*101dup rs776865643
NM_000176.3(NR3C1):c.*1055T>A rs886060051
NM_000176.3(NR3C1):c.*1087_*1088dup rs886060050
NM_000176.3(NR3C1):c.*1241C>T rs768128384
NM_000176.3(NR3C1):c.*1245_*1248dup rs10482710
NM_000176.3(NR3C1):c.*134G>A rs72466429
NM_000176.3(NR3C1):c.*1407A>G rs886060049
NM_000176.3(NR3C1):c.*1492A>G rs1812914163
NM_000176.3(NR3C1):c.*149T>C rs886060059
NM_000176.3(NR3C1):c.*1589A>G rs886060047
NM_000176.3(NR3C1):c.*2031C>T rs369162225
NM_000176.3(NR3C1):c.*2151A>C rs746282402
NM_000176.3(NR3C1):c.*2521T>A rs886060045
NM_000176.3(NR3C1):c.*2601A>T rs886060043
NM_000176.3(NR3C1):c.*2621T>G rs906319040
NM_000176.3(NR3C1):c.*2947T>G rs555242390
NM_000176.3(NR3C1):c.*3077G>A rs886060040
NM_000176.3(NR3C1):c.*3259G>A rs1812677304
NM_000176.3(NR3C1):c.*3378G>A rs1368015567
NM_000176.3(NR3C1):c.*3431G>C rs886060038
NM_000176.3(NR3C1):c.*3759dup rs772052566
NM_000176.3(NR3C1):c.*401dup rs886060058
NM_000176.3(NR3C1):c.*409del rs10482707
NM_000176.3(NR3C1):c.*409dup rs10482707
NM_000176.3(NR3C1):c.*534T>C rs924124147
NM_000176.3(NR3C1):c.*750del rs886060055
NM_000176.3(NR3C1):c.*766_*769dup rs34248080
NM_000176.3(NR3C1):c.*768_*769dup rs34248080
NM_000176.3(NR3C1):c.*769dup rs34248080
NM_000176.3(NR3C1):c.*834_*837dup rs886060053
NM_000176.3(NR3C1):c.*861_*868del rs547184962
NM_000176.3(NR3C1):c.*946T>G rs886060052
NM_000176.3(NR3C1):c.1018T>G (p.Ser340Ala) rs1839917064
NM_000176.3(NR3C1):c.1489A>G (p.Ile497Val) rs1818325449
NM_000176.3(NR3C1):c.2114A>G (p.Glu705Gly)
NM_000176.3(NR3C1):c.2282T>C (p.Ile761Thr) rs2151472803
NM_000176.3(NR3C1):c.2307C>G (p.Ile769Met) rs886060060
NM_000176.3(NR3C1):c.641G>A (p.Arg214Lys)
NM_000176.3(NR3C1):c.66_68delinsAAA (p.Arg23Lys) rs2151942107
NM_000176.3(NR3C1):c.946A>T (p.Met316Leu) rs1839935044
NM_001018077.1(NR3C1):c.-14+9T>C rs1462621396
NM_001018077.1(NR3C1):c.-363G>A rs1752038517
NM_001018077.1(NR3C1):c.-717A>T rs747240221
NM_001018077.1(NR3C1):c.-90A>G rs1752027227

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