List of variants in gene combination LOC125446261, MLC1 reported as likely benign

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: 26

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HGVS	dbSNP	gnomAD frequency
NM_015166.4(MLC1):c.231G>A (p.Pro77=)	rs150088744	0.00006
NM_015166.4(MLC1):c.178-13C>T	rs1569252040	0.00001
NM_015166.4(MLC1):c.183C>T (p.Cys61=)	rs1436214826	0.00001
NM_015166.4(MLC1):c.186C>T (p.Leu62=)	rs1314729155	0.00001
NM_015166.4(MLC1):c.198G>C (p.Ser66=)	rs199991229	0.00001
NM_015166.4(MLC1):c.207G>A (p.Ser69=)	rs2062188949	0.00001
NM_015166.4(MLC1):c.222C>T (p.Asn74=)	rs759148867	0.00001
NM_015166.4(MLC1):c.246C>T (p.Tyr82=)	rs373531536	0.00001
NM_015166.4(MLC1):c.267+18C>T	rs756282491	0.00001
NM_015166.4(MLC1):c.267+19G>A	rs754362648	0.00001
NM_015166.4(MLC1):c.267+9C>T	rs2146932553	0.00001
NM_015166.4(MLC1):c.178-11C>T	rs2518359167
NM_015166.4(MLC1):c.178-12G>A	rs757510976
NM_015166.4(MLC1):c.178-12G>T
NM_015166.4(MLC1):c.178-15_178-12dup	rs2518359205
NM_015166.4(MLC1):c.178-20A>T	rs1569252046
NM_015166.4(MLC1):c.178-9G>A	rs2146933516
NM_015166.4(MLC1):c.178-9G>C	rs2146933516
NM_015166.4(MLC1):c.201G>A (p.Gly67=)	rs2518358863
NM_015166.4(MLC1):c.207G>C (p.Ser69=)	rs2062188949
NM_015166.4(MLC1):c.207G>T (p.Ser69=)	rs2062188949
NM_015166.4(MLC1):c.213C>T (p.Tyr71=)	rs2062188802
NM_015166.4(MLC1):c.225G>C (p.Val75=)	rs1440820914
NM_015166.4(MLC1):c.267+16C>T	rs2518357861
NM_015166.4(MLC1):c.267+17A>G	rs2518357840
NM_015166.4(MLC1):c.267+18C>A	rs756282491

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