C0949595[trait identifier] AND "Juha Muilu Group; Institute for Molecu - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 56032	NM_000145.4(FSHR):c.1801C>G (p.Leu601Val)	FSHR (L575V +1 more)	Single nucleotide variant (missense variant)	Ovarian dysgenesis 1	GLikely pathogenic
Select item 29704	NM_000145.4(FSHR):c.1760C>A (p.Pro587His)	FSHR (P587H +1 more)	Single nucleotide variant (missense variant)	Ovarian dysgenesis 1	GPathogenic/Likely pathogenic
Select item 56031	NM_000145.4(FSHR):c.1724C>T (p.Ala575Val)	FSHR (A549V +1 more)	Single nucleotide variant (missense variant)	Ovarian dysgenesis 1	GLikely pathogenic
Select item 56030	NM_000145.4(FSHR):c.1043C>G (p.Pro348Arg)	FSHR (P322R +1 more)	Single nucleotide variant (missense variant)	Ovarian dysgenesis 1	GLikely pathogenic
Select item 56034	NM_000145.4(FSHR):c.671A>T (p.Asp224Val)	FSHR (D198V +1 more)	Single nucleotide variant (missense variant)	Ovarian dysgenesis 1	GLikely pathogenic
Select item 56033	NM_000145.4(FSHR):c.662T>G (p.Val221Gly)	FSHR (V195G +1 more)	Single nucleotide variant (missense variant)	Ovarian dysgenesis 1	GLikely pathogenic

ClinVar