ClinVar Miner

Submissions for variant NM_014832.5(TBC1D4):c.3617A>G (p.Asn1206Ser)

gnomAD frequency: 0.00958  dbSNP: rs76851570
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000118593 SCV000152999 benign not specified 2013-09-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004706543 SCV005232626 benign not provided criteria provided, single submitter not provided

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