Related gene-specific medical variations for Gene (Select 2063) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3300951	NM_005234.4(NR2F6):c.446C>T (p.Ser149Leu)	LOC130063917, NR2F6 (S149L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3201936	NM_005234.4(NR2F6):c.428C>T (p.Ser143Leu)	LOC130063917, NR2F6 (S143L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3201935	NM_005234.4(NR2F6):c.395C>T (p.Pro132Leu)	LOC130063917, NR2F6 (P132L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3201934	NM_005234.4(NR2F6):c.391A>G (p.Ile131Val)	LOC130063917, NR2F6 (I131V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3201933	NM_005234.4(NR2F6):c.385G>A (p.Gly129Ser)	LOC130063917, NR2F6 (G129S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510106	NM_005234.4(NR2F6):c.533C>T (p.Pro178Leu)	LOC130063916, NR2F6 (P178L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361267	NM_005234.4(NR2F6):c.443G>C (p.Gly148Ala)	LOC130063917, NR2F6 (G148A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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