List of variants in gene combination LHCGR, STON1-GTF2A1L reported as benign by Labcorp Genetics (formerly Invitae), Labcorp

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_000233.4(LHCGR):c.866+8G>A	rs6755901	0.81104
NM_000233.4(LHCGR):c.1065T>C (p.Asp355=)	rs11125179	0.51451
NM_000233.4(LHCGR):c.935A>G (p.Asn312Ser)	rs2293275	0.51043
NM_000233.4(LHCGR):c.872A>G (p.Asn291Ser)	rs12470652	0.03749
NM_000233.4(LHCGR):c.610C>T (p.Leu204=)	rs61996322	0.01070
NM_000233.4(LHCGR):c.1010T>C (p.Leu337Ser)	rs61996314	0.00677
NM_000233.4(LHCGR):c.622G>A (p.Val208Ile)	rs61996321	0.00614
NM_000233.4(LHCGR):c.606-5C>T	rs78135094	0.00283
NM_000233.4(LHCGR):c.458+3A>G	rs76210637	0.00251
NM_000233.4(LHCGR):c.458+17T>C	rs180853612	0.00131
NM_000233.4(LHCGR):c.1113T>C (p.Ile371=)	rs115267374	0.00099
NM_000233.4(LHCGR):c.1869T>C (p.Tyr623=)	rs144859947	0.00076
NM_000233.4(LHCGR):c.1953T>C (p.Tyr651=)	rs61996315	0.00070
NM_000233.4(LHCGR):c.680+9A>G	rs766301939	0.00008
NM_000233.4(LHCGR):c.1669G>A (p.Glu557Lys)	rs146785679	0.00005
NM_000233.4(LHCGR):c.114C>G (p.Pro38=)	rs74469055
NM_000233.4(LHCGR):c.50_55dup (p.Gln18_Pro19insLeuGln)	rs71245621

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