ClinVar Miner

Submissions for variant NM_001004067.4(NOMO3):c.1873C>T (p.Arg625Ter)

gnomAD frequency: 0.00001  dbSNP: rs1208366806
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
New York Genome Center RCV001254949 SCV001431031 uncertain significance not provided 2019-11-21 no assertion criteria provided clinical testing

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