ClinVar Miner

Submissions for variant NM_021926.4(ALX4):c.778-140G>C

gnomAD frequency: 0.57195  dbSNP: rs10769024
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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 RCV001549013 SCV001769066 benign Frontonasal dysplasia with alopecia and genital anomaly 2021-07-14 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001549014 SCV001769067 benign Parietal foramina 2 2021-07-14 criteria provided, single submitter clinical testing
GeneDx RCV001694091 SCV001906521 benign not provided 2018-10-16 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001694091 SCV005317912 benign not provided criteria provided, single submitter not provided

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