Related gene-specific medical variations for Gene (Select 121355) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3024514	NM_144594.3(GTSF1):c.221_222del (p.Arg74fs)	GPR84-AS1, GTSF1 (R74fs)	Deletion (frameshift variant)	Male infertility	GPathogenic
Select item 3024513	NM_144594.3(GTSF1):c.97C>A (p.His33Asn)	GPR84-AS1, GTSF1 (H33N)	Single nucleotide variant (missense variant)	Male infertility	GLikely pathogenic
Select item 2336503	NM_144594.3(GTSF1):c.112A>G (p.Arg38Gly)	GPR84-AS1, GTSF1 (R38G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316077	NM_144594.3(GTSF1):c.464C>T (p.Pro155Leu)	GPR84-AS1, GTSF1 (P155L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 712120	NM_144594.3(GTSF1):c.329-10C>T	GPR84-AS1, GTSF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 709454	NM_144594.3(GTSF1):c.348C>T (p.Ser116=)	GPR84-AS1, GTSF1	Single nucleotide variant (synonymous variant)	not provided	GBenign

ClinVar