ClinVar Miner

Submissions for variant NM_207391.3(RGS9BP):c.668C>T (p.Ala223Val)

gnomAD frequency: 0.02313  dbSNP: rs35413309
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000153840 SCV000203423 benign not specified 2014-03-19 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001518431 SCV001727120 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001518431 SCV005314284 benign not provided criteria provided, single submitter not provided

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