ClinVar Miner

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

Included ClinVar conditions (891):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
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HGVS dbSNP
NM_000901.4(NR3C2):c.*1032G>A rs61763141
NM_000901.4(NR3C2):c.*1410A>G rs5534
NM_000901.4(NR3C2):c.*2471G>A rs2871
NM_000901.4(NR3C2):c.-2C>G rs2070951
NM_000901.4(NR3C2):c.1497T>C (p.Asp499=) rs5525
NM_000901.4(NR3C2):c.1713T>C (p.Ser571=) rs5529
NM_000901.4(NR3C2):c.538G>A (p.Val180Ile) rs5522

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