List of variants in gene GNRHR reported as likely pathogenic for reproductive system disorder

Minimum submission review status:		Collection method:
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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000406.3(GNRHR):c.317A>G (p.Gln106Arg)	rs104893836	0.00234
NM_000406.3(GNRHR):c.785G>A (p.Arg262Gln)	rs104893837	0.00132
NM_000406.3(GNRHR):c.30T>A (p.Asn10Lys)	rs104893843	0.00006
NM_000406.3(GNRHR):c.797T>G (p.Leu266Arg)	rs148499544	0.00006
NM_000406.3(GNRHR):c.851A>G (p.Tyr284Cys)	rs28933074	0.00001
NM_000406.2(GNRHR):c.[416G>A];[806C>T]
NM_000406.3(GNRHR):c.351_352del (p.Ser118fs)
NM_000406.3(GNRHR):c.845C>T (p.Pro282Leu)
NM_000406.3(GNRHR):c.918CTT[2] (p.Phe309del)

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