ClinVar Miner

Submissions for variant NM_003672.4(CDC14A):c.1251-139A>G

gnomAD frequency: 0.93245  dbSNP: rs2270692
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
GeneDx RCV001539200 SCV001756944 benign not provided 2018-11-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001554861 SCV001776180 benign Autosomal recessive nonsyndromic hearing loss 32 2021-07-14 criteria provided, single submitter clinical testing

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