ClinVar Miner

Submissions for variant NM_001370298.3(FGD4):c.2046+37A>G

gnomAD frequency: 0.34250  dbSNP: rs7970584
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001669912 SCV001890409 benign not provided 2018-06-23 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001702232 SCV001933440 benign Charcot-Marie-Tooth disease type 4H 2021-08-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001669912 SCV005236950 benign not provided criteria provided, single submitter not provided

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