ClinVar for MedGen (Select 349670) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 208793	NC_000004.12:g.73436164C>A	AFP, LOC111832670	Single nucleotide variant	Alpha-fetoprotein, hereditary persistence of	GAffects
Select item 18168	NC_000004.12:g.73436100G>A	AFP, LOC111832670	Single nucleotide variant	Alpha-fetoprotein, hereditary persistence of	GAffects