ClinVar Miner

Submissions for variant NM_015272.5(RPGRIP1L):c.1892C>T (p.Thr631Ile)

dbSNP: rs1567841081
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Gharavi Laboratory, Columbia University RCV000723021 SCV000854152 uncertain significance not provided 2018-09-16 no assertion criteria provided research
Natera, Inc. RCV001279162 SCV001466244 uncertain significance Familial aplasia of the vermis 2020-08-17 no assertion criteria provided clinical testing

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