ClinVar Miner

Submissions for variant NM_000176.3(NR3C1):c.2035G>A (p.Gly679Ser)

dbSNP: rs104893914
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV000017540 SCV005671077 uncertain significance Glucocorticoid resistance 2024-05-13 criteria provided, single submitter clinical testing
OMIM RCV000017540 SCV000037812 pathogenic Glucocorticoid resistance 2005-06-01 no assertion criteria provided literature only

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