List of variants in gene GNRHR reported by OMIM

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: 14

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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.416G>A (p.Arg139His)	rs104893842	0.00021
NM_000406.3(GNRHR):c.30T>A (p.Asn10Lys)	rs104893843	0.00006
NM_000406.3(GNRHR):c.268G>A (p.Glu90Lys)	rs104893844	0.00001
NM_000406.3(GNRHR):c.851A>G (p.Tyr284Cys)	rs28933074	0.00001
NM_000406.3(GNRHR):c.386C>A (p.Ala129Asp)	rs104893838
NM_000406.3(GNRHR):c.504T>A (p.Ser168Arg)	rs104893840
NM_000406.3(GNRHR):c.511G>A (p.Ala171Thr)	rs74452732
NM_000406.3(GNRHR):c.523-1G>A	rs797044452
NM_000406.3(GNRHR):c.651C>A (p.Ser217Arg)	rs104893839
NM_000406.3(GNRHR):c.941T>A (p.Leu314Ter)	rs104893841
NM_000406.3(GNRHR):c.959C>T (p.Pro320Leu)	rs104893847
NM_001012763.1(GNRHR):c.30_31delinsAA (p.Asn10_Gln11delinsLysLys)	rs281865427

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