List of variants in gene combination LHCGR, STON1-GTF2A1L reported by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000233.4(LHCGR):c.605+52del	rs111834744	0.11909
NM_000233.4(LHCGR):c.610C>T (p.Leu204=)	rs61996322	0.01070
NM_000233.4(LHCGR):c.458+3A>G	rs76210637	0.00251
NM_000233.4(LHCGR):c.1847C>A (p.Ser616Tyr)	rs121912525	0.00005
NM_000233.4(LHCGR):c.1060G>A (p.Glu354Lys)	rs121912529
NM_000233.4(LHCGR):c.1732G>T (p.Asp578Tyr)	rs121912532
NM_000233.4(LHCGR):c.211G>C (p.Gly71Arg)
NM_000233.4(LHCGR):c.562G>T (p.Glu188Ter)	rs2529810344

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