ClinVar Miner

List of variants in gene NR3C2 studied for abdominal and pelvic region disorder

Included ClinVar conditions (961):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 151
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HGVS dbSNP
NM_000901.4(NR3C2):c.*2581C>T rs146849424
NM_000901.5(NR3C2):c.*1019C>G
NM_000901.5(NR3C2):c.*1032G>A rs61763141
NM_000901.5(NR3C2):c.*1032G>C rs61763141
NM_000901.5(NR3C2):c.*1088C>T
NM_000901.5(NR3C2):c.*1110C>G
NM_000901.5(NR3C2):c.*1121T>C rs114071155
NM_000901.5(NR3C2):c.*1165C>T rs5533
NM_000901.5(NR3C2):c.*1206G>C rs557553789
NM_000901.5(NR3C2):c.*1209G>A rs118144639
NM_000901.5(NR3C2):c.*124G>C
NM_000901.5(NR3C2):c.*1290G>A
NM_000901.5(NR3C2):c.*1307C>G rs886059125
NM_000901.5(NR3C2):c.*1327C>A rs879593672
NM_000901.5(NR3C2):c.*1352G>A
NM_000901.5(NR3C2):c.*1365G>A rs550508714
NM_000901.5(NR3C2):c.*1406A>T rs61763137
NM_000901.5(NR3C2):c.*1410A>G rs5534
NM_000901.5(NR3C2):c.*1452C>T rs181282602
NM_000901.5(NR3C2):c.*1465G>A rs886059124
NM_000901.5(NR3C2):c.*1471A>G
NM_000901.5(NR3C2):c.*1475T>G rs886059123
NM_000901.5(NR3C2):c.*1491G>A
NM_000901.5(NR3C2):c.*1493C>T rs886059122
NM_000901.5(NR3C2):c.*1493del rs533687617
NM_000901.5(NR3C2):c.*1508A>G rs5535
NM_000901.5(NR3C2):c.*1541_*1544dup rs140789678
NM_000901.5(NR3C2):c.*1667_*1670TTTG[1] rs146592484
NM_000901.5(NR3C2):c.*1726_*1729dup rs199601327
NM_000901.5(NR3C2):c.*1758A>G rs886059121
NM_000901.5(NR3C2):c.*1774A>G rs377659495
NM_000901.5(NR3C2):c.*1797A>G
NM_000901.5(NR3C2):c.*1802G>A rs5536
NM_000901.5(NR3C2):c.*1836_*1839ATTA[1] rs570043057
NM_000901.5(NR3C2):c.*1905_*1907dup rs886059120
NM_000901.5(NR3C2):c.*2065A>C rs72647600
NM_000901.5(NR3C2):c.*2088G>A rs145711262
NM_000901.5(NR3C2):c.*2289T>G
NM_000901.5(NR3C2):c.*2296T>C
NM_000901.5(NR3C2):c.*2345T>C rs886059119
NM_000901.5(NR3C2):c.*2354T>C rs886059118
NM_000901.5(NR3C2):c.*2368C>A rs886059117
NM_000901.5(NR3C2):c.*2384T>C
NM_000901.5(NR3C2):c.*2388T>C rs5537
NM_000901.5(NR3C2):c.*2410T>C rs186309103
NM_000901.5(NR3C2):c.*2471G>A rs2871
NM_000901.5(NR3C2):c.*2578T>G
NM_000901.5(NR3C2):c.*324C>T rs886059128
NM_000901.5(NR3C2):c.*325G>A rs201950852
NM_000901.5(NR3C2):c.*356A>G
NM_000901.5(NR3C2):c.*379G>A
NM_000901.5(NR3C2):c.*412C>T rs17024360
NM_000901.5(NR3C2):c.*416T>C rs886059127
NM_000901.5(NR3C2):c.*442_*444del rs769087750
NM_000901.5(NR3C2):c.*474_*475insTAA rs886059126
NM_000901.5(NR3C2):c.*519G>A
NM_000901.5(NR3C2):c.*586G>A
NM_000901.5(NR3C2):c.*592G>A rs751325270
NM_000901.5(NR3C2):c.*6C>T rs373627783
NM_000901.5(NR3C2):c.*755A>C rs5532
NM_000901.5(NR3C2):c.*7G>A
NM_000901.5(NR3C2):c.*804G>T rs72648707
NM_000901.5(NR3C2):c.*813G>A
NM_000901.5(NR3C2):c.*86T>C rs5530
NM_000901.5(NR3C2):c.*890T>G rs72648706
NM_000901.5(NR3C2):c.*90A>G
NM_000901.5(NR3C2):c.*924C>T
NM_000901.5(NR3C2):c.-111C>T rs886059132
NM_000901.5(NR3C2):c.-14C>G rs886059131
NM_000901.5(NR3C2):c.-213G>A rs571381864
NM_000901.5(NR3C2):c.-228T>C rs553066220
NM_000901.5(NR3C2):c.-238C>T
NM_000901.5(NR3C2):c.-243G>T
NM_000901.5(NR3C2):c.-249C>T rs886059133
NM_000901.5(NR3C2):c.-2C>G rs2070951
NM_000901.5(NR3C2):c.-3+10G>A rs72646913
NM_000901.5(NR3C2):c.-5C>A
NM_000901.5(NR3C2):c.-8A>T rs61760021
NM_000901.5(NR3C2):c.100A>G (p.Thr34Ala)
NM_000901.5(NR3C2):c.103G>C (p.Glu35Gln) rs141860706
NM_000901.5(NR3C2):c.1055C>A (p.Ser352Tyr)
NM_000901.5(NR3C2):c.1090A>T (p.Thr364Ser)
NM_000901.5(NR3C2):c.1092G>A (p.Thr364=) rs61729559
NM_000901.5(NR3C2):c.1131dup (p.Glu378Ter) rs1560735659
NM_000901.5(NR3C2):c.1272A>G (p.Ser424=)
NM_000901.5(NR3C2):c.1308T>A (p.Cys436Ter) rs121912570
NM_000901.5(NR3C2):c.1331A>C (p.Asn444Thr)
NM_000901.5(NR3C2):c.1380T>A (p.Phe460Leu)
NM_000901.5(NR3C2):c.1398T>C (p.Tyr466=) rs5524
NM_000901.5(NR3C2):c.1409C>A (p.Ser470Ter) rs879255348
NM_000901.5(NR3C2):c.1497T>C (p.Asp499=) rs5525
NM_000901.5(NR3C2):c.1513G>A (p.Glu505Lys)
NM_000901.5(NR3C2):c.1559G>T (p.Gly520Val) rs754916440
NM_000901.5(NR3C2):c.1609C>T (p.Arg537Ter) rs121912562
NM_000901.5(NR3C2):c.1661A>G (p.Asn554Ser) rs5527
NM_000901.5(NR3C2):c.1686A>C (p.Ser562=)
NM_000901.5(NR3C2):c.1689C>T (p.His563=) rs5528
NM_000901.5(NR3C2):c.1705A>G (p.Arg569Gly) rs61759976
NM_000901.5(NR3C2):c.1713T>C (p.Ser571=) rs5529
NM_000901.5(NR3C2):c.1757+6T>C
NM_000901.5(NR3C2):c.1791A>G (p.Ser597=) rs34905604
NM_000901.5(NR3C2):c.1897G>A (p.Gly633Arg) rs121912566
NM_000901.5(NR3C2):c.1935C>A (p.Cys645Ter) rs121912564
NM_000901.5(NR3C2):c.2017C>T (p.Arg673Ter) rs121912571
NM_000901.5(NR3C2):c.2024C>G (p.Ser675Ter) rs121912572
NM_000901.5(NR3C2):c.2055C>A (p.His685Gln)
NM_000901.5(NR3C2):c.2087C>T (p.Pro696Leu) rs368322580
NM_000901.5(NR3C2):c.2091A>C (p.Pro697=)
NM_000901.5(NR3C2):c.2096del (p.Pro699fs) rs748573472
NM_000901.5(NR3C2):c.2097A>C (p.Pro699=)
NM_000901.5(NR3C2):c.2102C>G (p.Pro701Arg) rs754694314
NM_000901.5(NR3C2):c.2126C>T (p.Thr709Met) rs139938639
NM_000901.5(NR3C2):c.2139T>C (p.Pro713=) rs151096115
NM_000901.5(NR3C2):c.215C>G (p.Pro72Arg)
NM_000901.5(NR3C2):c.2178G>A (p.Gln726=) rs144234574
NM_000901.5(NR3C2):c.218G>A (p.Cys73Tyr)
NM_000901.5(NR3C2):c.2312G>A (p.Arg771His) rs143057152
NM_000901.5(NR3C2):c.2327A>G (p.Gln776Arg) rs121912565
NM_000901.5(NR3C2):c.2334C>T (p.Ile778=)
NM_000901.5(NR3C2):c.2365+3del rs1560949756
NM_000901.5(NR3C2):c.2412T>C (p.Tyr804=) rs548602386
NM_000901.5(NR3C2):c.2453C>T (p.Ser818Leu) rs121912573
NM_000901.5(NR3C2):c.2578G>A (p.Val860Ile) rs147398624
NM_000901.5(NR3C2):c.2657T>G (p.Leu886Arg) rs1560928649
NM_000901.5(NR3C2):c.2745G>A (p.Gly915=)
NM_000901.5(NR3C2):c.2755C>T (p.Gln919Ter) rs1553986377
NM_000901.5(NR3C2):c.2771T>C (p.Leu924Pro) rs121912563
NM_000901.5(NR3C2):c.2809G>A (p.Asp937Asn) rs886059129
NM_000901.5(NR3C2):c.2839C>T (p.Arg947Ter) rs121912569
NM_000901.5(NR3C2):c.2871C>T (p.Pro957=)
NM_000901.5(NR3C2):c.2871dup (p.Ala958fs) rs1560910156
NM_000901.5(NR3C2):c.2915A>G (p.Glu972Gly) rs121912574
NM_000901.5(NR3C2):c.2936T>C (p.Leu979Pro) rs121912567
NM_000901.5(NR3C2):c.334G>C (p.Val112Leu)
NM_000901.5(NR3C2):c.405G>C (p.Gln135His)
NM_000901.5(NR3C2):c.449G>A (p.Arg150His) rs13306591
NM_000901.5(NR3C2):c.488C>G (p.Ser163Ter) rs121912568
NM_000901.5(NR3C2):c.534C>T (p.Arg178=) rs201996429
NM_000901.5(NR3C2):c.538G>A (p.Val180Ile) rs5522
NM_000901.5(NR3C2):c.739A>T (p.Arg247Trp) rs149902988
NM_000901.5(NR3C2):c.747C>T (p.His249=) rs886059130
NM_000901.5(NR3C2):c.767A>G (p.Asn256Ser)
NM_000901.5(NR3C2):c.822C>A (p.Ser274Arg)
NM_000901.5(NR3C2):c.934A>G (p.Ser312Gly)
NM_001354819.1(NR3C2):c.-3+2021C>G rs749300160
NM_001354819.1(NR3C2):c.-3+2041C>T rs886059134
NM_001354819.1(NR3C2):c.-3+2091TGCCCC[2] rs540712695
NM_001354819.1(NR3C2):c.-3+2094C>T rs61760022
NR3C2, 1-BP DEL, 1226G
NR3C2, 1-BP DEL, 1597T
NR3C2, 8-BP DEL, NT537

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