"PROKR2-related condition"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2886691	NM_144773.4(PROKR2):c.1069C>T (p.Arg357Trp)	PROKR2 (R357W)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 338853	NM_144773.4(PROKR2):c.1005G>A (p.Thr335=)	PROKR2	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 2637063	NM_144773.4(PROKR2):c.946T>C (p.Tyr316His)	PROKR2 (Y316H)	Single nucleotide variant (missense variant)	PROKR2-related condition	GUncertain significance
Select item 2630400	NM_144773.4(PROKR2):c.770G>T (p.Gly257Val)	PROKR2 (G257V)	Single nucleotide variant (missense variant)	PROKR2-related condition	GUncertain significance
Select item 338860	NM_144773.4(PROKR2):c.390C>T (p.Ser130=)	PROKR2	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +3 more	GLikely benign
Select item 2182552	NM_144773.4(PROKR2):c.381C>G (p.Leu127=)	PROKR2	Single nucleotide variant (synonymous variant)	PROKR2-related condition +1 more	GLikely benign
Select item 156563	NM_144773.4(PROKR2):c.343G>A (p.Val115Met)	PROKR2 (V115M)	Single nucleotide variant (missense variant)	PROKR2-related condition	GUncertain significance
Select item 3451	NM_144773.4(PROKR2):c.254G>A (p.Arg85His)	PROKR2 (R85H)	Single nucleotide variant (missense variant)	PROKR2-related condition +4 more	GConflicting classifications of pathogenicity

ClinVar