List of variants in gene FSHR reported as likely pathogenic for Ovarian dysgenesis 1

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000145.4(FSHR):c.1043C>G (p.Pro348Arg)	rs386833510	0.00001
NM_000145.4(FSHR):c.1384G>C (p.Ala462Pro)	rs1674323340
NM_000145.4(FSHR):c.1724C>T (p.Ala575Val)	rs386833511
NM_000145.4(FSHR):c.1760C>A (p.Pro587His)	rs386833512
NM_000145.4(FSHR):c.1801C>G (p.Leu601Val)	rs386833513
NM_000145.4(FSHR):c.1862C>T (p.Ala621Val)	rs1674297842
NM_000145.4(FSHR):c.662T>G (p.Val221Gly)	rs386833514
NM_000145.4(FSHR):c.671A>T (p.Asp224Val)	rs386833515

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