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

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_000191.3(HMGCL):c.244G>A (p.Val82Ile)	rs538620811	0.00007
NM_000191.3(HMGCL):c.720A>G (p.Gln240=)	rs911190800	0.00005
NM_000191.3(HMGCL):c.828G>A (p.Leu276=)	rs771024022	0.00002
NM_000191.3(HMGCL):c.501C>T (p.Tyr167=)	rs200189529	0.00001
NM_000191.3(HMGCL):c.624G>A (p.Val208=)	rs747724373	0.00001
NM_000191.3(HMGCL):c.528T>C (p.Tyr176=)	rs112508527
NM_000191.3(HMGCL):c.630C>T (p.Thr210=)	rs886046313
NM_000191.3(HMGCL):c.708C>T (p.Asp236=)	rs886046312
NM_000191.3(HMGCL):c.750+14T>A	rs778868742
NM_000191.3(HMGCL):c.765C>T (p.Val255=)	rs778296169
NM_000191.3(HMGCL):c.795C>G (p.Gly265=)	rs1488079271

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