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

Submission 1 (benign) minimum review status:		Submission 1 (benign) 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_012213.3(MLYCD):c.1464A>G (p.Gln488=)	rs1127368	0.00870
NM_012213.3(MLYCD):c.206C>T (p.Ala69Val)	rs200579941	0.00284
NM_012213.3(MLYCD):c.776G>C (p.Gly259Ala)	rs77493891	0.00265
NM_012213.3(MLYCD):c.393C>T (p.Tyr131=)	rs560831102	0.00015

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