List of variants in gene combination LOC125446261, MLC1 reported as pathogenic by Labcorp Genetics (formerly Invitae), Labcorp

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_015166.4(MLC1):c.178-10T>A	rs80358243	0.00001
NM_015166.4(MLC1):c.206C>T (p.Ser69Leu)	rs281875309	0.00001
NM_015166.4(MLC1):c.251G>A (p.Arg84His)	rs1425784992	0.00001
NM_015166.4(MLC1):c.218G>A (p.Gly73Glu)	rs1602063709
NM_015166.4(MLC1):c.267+1G>A	rs2518357998

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