List of variants in gene MLC1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_015166.4(MLC1):c.279G>A (p.Ser93=)	rs11568172	0.00422
NM_015166.4(MLC1):c.*1499C>T	rs144067372	0.00332
NM_015166.4(MLC1):c.627C>T (p.Ala209=)	rs138153307	0.00070
NM_015166.4(MLC1):c.105C>T (p.Ser35=)	rs573095096	0.00003
NM_015166.4(MLC1):c.858C>T (p.Ile286=)	rs140824687	0.00003
NM_015166.4(MLC1):c.1011T>G (p.Gly337=)
NM_015166.4(MLC1):c.654C>A (p.Asn218Lys)	rs41302601
NM_015166.4(MLC1):c.654C>T (p.Asn218=)	rs41302601

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