ClinVar Miner

List of variants in gene NR3C2 reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (956):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 42
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HGVS dbSNP
NM_000901.4(NR3C2):c.*2581C>T rs146849424
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.*1452C>T rs181282602
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.*1774A>G rs377659495
NM_000901.5(NR3C2):c.*1802G>A rs5536
NM_000901.5(NR3C2):c.*1836_*1839ATTA[1] rs570043057
NM_000901.5(NR3C2):c.*2065A>C rs72647600
NM_000901.5(NR3C2):c.*2088G>A rs145711262
NM_000901.5(NR3C2):c.*2388T>C rs5537
NM_000901.5(NR3C2):c.*2410T>C rs186309103
NM_000901.5(NR3C2):c.*325G>A rs201950852
NM_000901.5(NR3C2):c.*412C>T rs17024360
NM_000901.5(NR3C2):c.*755A>C rs5532
NM_000901.5(NR3C2):c.*804G>T rs72648707
NM_000901.5(NR3C2):c.*86T>C rs5530
NM_000901.5(NR3C2):c.*890T>G rs72648706
NM_000901.5(NR3C2):c.-213G>A rs571381864
NM_000901.5(NR3C2):c.-3+10G>A rs72646913
NM_000901.5(NR3C2):c.-8A>T rs61760021
NM_000901.5(NR3C2):c.103G>C (p.Glu35Gln) rs141860706
NM_000901.5(NR3C2):c.1092G>A (p.Thr364=) rs61729559
NM_000901.5(NR3C2):c.1398T>C (p.Tyr466=) rs5524
NM_000901.5(NR3C2):c.1661A>G (p.Asn554Ser) rs5527
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.1791A>G (p.Ser597=) rs34905604
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.2178G>A (p.Gln726=) rs144234574
NM_000901.5(NR3C2):c.2312G>A (p.Arg771His) rs143057152
NM_000901.5(NR3C2):c.2412T>C (p.Tyr804=) rs548602386
NM_000901.5(NR3C2):c.2578G>A (p.Val860Ile) rs147398624
NM_000901.5(NR3C2):c.449G>A (p.Arg150His) rs13306591
NM_001354819.1(NR3C2):c.-3+2091TGCCCC[2] rs540712695
NM_001354819.1(NR3C2):c.-3+2094C>T rs61760022

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