ClinVar Miner

Submissions for variant NM_153676.4(USH1C):c.1570C>T (p.Pro524Ser)

gnomAD frequency: 0.00001  dbSNP: rs576189967
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000734150 SCV000862272 uncertain significance not provided 2018-07-10 criteria provided, single submitter clinical testing

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