Related gene-specific medical variations for Gene (Select 137872) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3273142	NM_144650.3(ADHFE1):c.17G>A (p.Arg6Gln)	ADHFE1, LOC130000529 (R6Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379263	NM_144650.3(ADHFE1):c.25G>C (p.Val9Leu)	ADHFE1, LOC130000529 (V9L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance