List of variants in gene combination LHCGR, STON1-GTF2A1L reported as likely benign 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000233.4(LHCGR):c.568C>A (p.Gln190Lys)	rs61996318	0.00163
NM_000233.4(LHCGR):c.161+9A>G	rs573699597	0.00031
NM_000233.4(LHCGR):c.426G>A (p.Thr142=)	rs142554296	0.00019
NM_000233.4(LHCGR):c.54G>A (p.Gln18=)	rs780848944	0.00013
NM_001198593.2(STON1-GTF2A1L):c.3442-20603G>A	rs779799454	0.00003
NM_000233.4(LHCGR):c.605+8T>C	rs1553392347	0.00002
NM_000233.4(LHCGR):c.337T>A (p.Tyr113Asn)	rs140691492

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