ClinVar Miner

Submissions for variant NM_001368397.1(FRMPD4):c.3937C>A (p.Arg1313=)

dbSNP: rs41303149
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000723906 SCV000202752 uncertain significance not provided 2014-02-20 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000153276 SCV000594895 likely benign not specified 2015-10-29 criteria provided, single submitter clinical testing
Center for Human Genetics, Inc, Center for Human Genetics, Inc RCV000659681 SCV000781526 likely benign Autism, susceptibility to, X-linked 4 2016-11-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000723906 SCV001054227 benign not provided 2019-12-31 criteria provided, single submitter clinical testing

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