Related gene-specific medical variations for Gene (Select 11282) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3125926	NM_014275.5(MGAT4B):c.142G>A (p.Asp48Asn)	LOC129995444, MGAT4B (D48N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229913	NM_014275.5(MGAT4B):c.58C>T (p.Leu20Phe)	MGAT4B, SQSTM1 (L20F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance