Variants in gene HMGCL with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 4

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HGVS	dbSNP	gnomAD frequency
NM_000191.3(HMGCL):c.61-17C>T	rs56913973	0.00337
NM_000191.3(HMGCL):c.393A>G (p.Ser131=)	rs56218308	0.00275
NM_000191.3(HMGCL):c.443A>G (p.Gln148Arg)	rs192833530	0.00070
NM_000191.3(HMGCL):c.375C>T (p.Val125=)	rs139102957	0.00009

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