ClinVar Miner

List of variants in gene combination LHCGR, STON1-GTF2A1L reported as likely pathogenic 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000233.4(LHCGR):c.1178T>G (p.Val393Gly)	rs1394300572	0.00001
NM_000233.4(LHCGR):c.1733A>C (p.Asp578Ala)	rs121912518

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