C0949595[trait identifier] AND "GenomeConnect, ClinGen"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1339879	NM_000145.4(FSHR):c.1669C>T (p.Arg557Trp)	FSHR (R531W +1 more)	Single nucleotide variant (missense variant)	Ovarian hyperstimulation syndrome +1 more	Gnot provided
Select item 1339880	NM_000145.4(FSHR):c.1501G>A (p.Ala501Thr)	FSHR (A475T +1 more)	Single nucleotide variant (missense variant)	Ovarian hyperstimulation syndrome +1 more	Gnot provided