ClinVar Miner

Submissions for variant NM_003923.3(FOXH1):c.468G>A (p.Pro156=)

gnomAD frequency: 0.00001  dbSNP: rs777440236
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001421179 SCV001623701 likely benign Holoprosencephaly sequence 2018-02-01 criteria provided, single submitter clinical testing

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