List of variants in gene combination LHCGR, STON1-GTF2A1L reported as likely benign by GeneDx

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000233.4(LHCGR):c.866+25C>T	rs147917820	0.01273
NM_000233.4(LHCGR):c.610C>T (p.Leu204=)	rs61996322	0.01070
NM_000233.4(LHCGR):c.*131C>T	rs73928204	0.00766
NM_000233.4(LHCGR):c.622G>A (p.Val208Ile)	rs61996321	0.00614
NM_000233.4(LHCGR):c.309-55T>C	rs143404304	0.00531
NM_000233.4(LHCGR):c.606-5C>T	rs78135094	0.00283
NM_000233.4(LHCGR):c.867-176A>C	rs113455986	0.00272
NM_000233.4(LHCGR):c.1669G>A (p.Glu557Lys)	rs146785679	0.00005
NM_000233.4(LHCGR):c.*53dup	rs200887026
NM_000233.4(LHCGR):c.606-268G>A	rs111338389

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