Related gene-specific medical variations for Gene (Select 285704) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3313995	NM_001366508.1(RGMB):c.343C>T (p.Leu115Phe)	LOC126807464, RGMB (L115F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153609	NM_001366508.1(RGMB):c.388A>G (p.Thr130Ala)	LOC126807464, RGMB (T171A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2622888	NM_001366508.1(RGMB):c.607C>A (p.Pro203Thr)	LOC126807464, RGMB (P243T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600810	NM_001366508.1(RGMB):c.220G>A (p.Val74Ile)	LOC126807464, RGMB (V114I +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2550617	NM_001366508.1(RGMB):c.346A>G (p.Met116Val)	LOC126807464, RGMB (M116V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474501	NM_001366508.1(RGMB):c.167T>C (p.Ile56Thr)	LOC126807464, RGMB (I97T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372016	NM_001366508.1(RGMB):c.395C>G (p.Pro132Arg)	LOC126807464, RGMB (P132R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324230	NM_001366508.1(RGMB):c.530A>T (p.Asn177Ile)	LOC126807464, RGMB (N217I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar