Related gene-specific medical variations for Gene (Select 126805826) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3081564	NM_024901.5(DENND2D):c.1322G>C (p.Ser441Thr)	DENND2D, LOC126805826 (S438T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081563	NM_024901.5(DENND2D):c.1193C>A (p.Ala398Glu)	DENND2D, LOC126805826 (A398E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594384	NM_024901.5(DENND2D):c.1220G>T (p.Arg407Ile)	DENND2D, LOC126805826 (R404I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589245	NM_024901.5(DENND2D):c.1117G>A (p.Glu373Lys)	DENND2D, LOC126805826 (E370K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2263127	NM_024901.5(DENND2D):c.1219A>G (p.Arg407Gly)	DENND2D, LOC126805826 (R407G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215223	NM_024901.5(DENND2D):c.1172C>T (p.Ala391Val)	DENND2D, LOC126805826 (A391V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar