ClinVar Miner

Submissions for variant NM_021926.4(ALX4):c.778-117T>C

gnomAD frequency: 0.79676  dbSNP: rs10742699
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001549011 SCV001769064 benign Frontonasal dysplasia with alopecia and genital anomaly 2021-07-14 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001549012 SCV001769065 benign Parietal foramina 2 2021-07-14 criteria provided, single submitter clinical testing
GeneDx RCV001685504 SCV001900140 benign not provided 2018-10-16 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001685504 SCV005317909 benign not provided criteria provided, single submitter not provided

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