List of variants in gene FSHR reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

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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.485G>A (p.Arg162Lys)	rs111883853	0.00372
NM_000145.4(FSHR):c.24G>T (p.Leu8Phe)	rs115030945	0.00034
NM_000145.4(FSHR):c.312G>A (p.Lys104=)	rs147355964	0.00018
NM_000145.4(FSHR):c.594-45T>C	rs201378858	0.00012
NM_000145.4(FSHR):c.1752C>T (p.Cys584=)
NM_000145.4(FSHR):c.603C>T (p.Ser201=)	rs75552966
NM_000145.4(FSHR):c.987G>T (p.Thr329=)

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