ClinVar Miner

Submissions for variant NM_182894.3(VSX2):c.455G>A (p.Arg152Lys)

dbSNP: rs1566883262
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV000678660 SCV000804752 uncertain significance Retinitis pigmentosa 2016-09-01 no assertion criteria provided clinical testing

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