ClinVar Miner

List of variants reported as likely pathogenic for Heterotaxy, visceral, 5, autosomal by Labcorp Genetics (formerly Invitae), Labcorp

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_018055.5(NODAL):c.891+1G>A	rs878855044	0.00001
NM_018055.5(NODAL):c.891+2T>A	rs1564667078

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