ClinVar Miner

Submissions for variant NM_000142.5(FGFR3):c.335G>A (p.Arg112Gln)

gnomAD frequency: 0.00008  dbSNP: rs758163128
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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) RCV000394407 SCV000345468 uncertain significance not provided 2016-09-12 criteria provided, single submitter clinical testing
GeneDx RCV000394407 SCV001804300 likely benign not provided 2020-10-13 criteria provided, single submitter clinical testing
Invitae RCV000394407 SCV002507819 likely benign not provided 2023-12-24 criteria provided, single submitter clinical testing

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