List of variants in gene MED13L reported as likely benign by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_015335.5(MED13L):c.4691C>T (p.Pro1564Leu)	rs112709561	0.00041
NM_015335.5(MED13L):c.4697C>T (p.Ser1566Leu)	rs113890513	0.00032
NM_015335.5(MED13L):c.1072A>G (p.Thr358Ala)	rs1193527567	0.00001
NM_015335.5(MED13L):c.881_882insAATCCCGGT (p.Val294_Pro295insIleProVal)	rs2499943835

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