List of variants in gene MED13L reported as uncertain significance by Baylor Genetics

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_015335.5(MED13L):c.1656A>G (p.Ile552Met)	rs746110094
NM_015335.5(MED13L):c.217C>T (p.Arg73Cys)
NM_015335.5(MED13L):c.2240C>T (p.Ser747Leu)	rs368050346
NM_015335.5(MED13L):c.3524A>G (p.Asn1175Ser)
NM_015335.5(MED13L):c.4190C>T (p.Ser1397Leu)	rs2137287209
NM_015335.5(MED13L):c.443G>A (p.Arg148Gln)	rs1461395322
NM_015335.5(MED13L):c.5659G>A (p.Val1887Ile)	rs201002721
NM_015335.5(MED13L):c.970C>T (p.Pro324Ser)	rs1183900324

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