ClinVar Miner

List of variants reported as likely pathogenic for Visceral heterotaxy 5, autosomal

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Total variants: 3
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HGVS dbSNP
NM_018055.5(NODAL):c.194-1G>T rs1564667617
NM_018055.5(NODAL):c.700_707del (p.Arg234fs) rs1564667180
NM_018055.5(NODAL):c.891+1G>A rs878855044

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