List of variants in gene MLC1 reported as likely benign by Illumina Laboratory Services, Illumina

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_015166.4(MLC1):c.*215C>T	rs148160537	0.00690
NM_015166.4(MLC1):c.*414C>T	rs12484303	0.00577
NM_015166.4(MLC1):c.*860A>C	rs41283492	0.00426
NM_015166.4(MLC1):c.*1689T>G	rs188855026	0.00406
NM_015166.4(MLC1):c.*1499C>T	rs144067372	0.00332
NM_015166.4(MLC1):c.*660C>T	rs139148001	0.00263
NM_015166.4(MLC1):c.*2051G>A	rs540245725	0.00004
NM_015166.3(MLC1):c.-414G>A	rs543054100	0.00002
NM_015166.4(MLC1):c.*1368dup	rs200990035
NM_015166.4(MLC1):c.*1981dup	rs145385166
NM_015166.4(MLC1):c.377_378insGGGGGTC	rs141063000
NM_015166.4(MLC1):c.*431C>T	rs114598884

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