ClinVar Miner

Submissions for variant NM_153676.4(USH1C):c.966G>C (p.Arg322=)

gnomAD frequency: 0.00001  dbSNP: rs748749433
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
Eurofins Ntd Llc (ga) RCV000728053 SCV000855578 uncertain significance not provided 2017-07-25 criteria provided, single submitter clinical testing
Invitae RCV000728053 SCV002354962 likely benign not provided 2022-11-15 criteria provided, single submitter clinical testing

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