List of variants in gene FSHR reported as benign 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000145.4(FSHR):c.2039G>A (p.Ser680Asn)	rs6166	0.56644
NM_000145.4(FSHR):c.919G>A (p.Ala307Thr)	rs6165	0.47188
NM_000145.4(FSHR):c.-29G>A	rs1394205	0.27960
NM_000145.4(FSHR):c.*256C>T	rs72873077	0.02778

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