List of variants in gene combination LHCGR, STON1-GTF2A1L reported as likely pathogenic 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
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000233.4(LHCGR):c.29T>C (p.Leu10Pro)	rs917607255	0.00001
NM_000233.4(LHCGR):c.32T>C (p.Leu11Pro)	rs755654915
NM_000233.4(LHCGR):c.370C>T (p.Arg124Ter)	rs773279269

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