ClinVar Miner

Submissions for variant NM_021005.4(NR2F2):c.103_109del (p.Gly35fs)

dbSNP: rs1899167400
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV001784665 SCV002020159 likely pathogenic not provided 2019-12-05 criteria provided, single submitter clinical testing
OMIM RCV001171518 SCV001334302 pathogenic 46,xx sex reversal 5 2020-06-02 no assertion criteria provided literature only

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