ClinVar Miner

Submissions for variant NM_000996.4(RPL35A):c.184G>T (p.Gly62Cys)

gnomAD frequency: 0.00003  dbSNP: rs146882967
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001437575 SCV001640431 likely benign Diamond-Blackfan anemia 5 2018-06-12 criteria provided, single submitter clinical testing

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