List of variants in gene MED25 reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_030973.4(MED25):c.1438C>G (p.Leu480Val)	rs148214958	0.00011
NM_030973.4(MED25):c.395G>A (p.Arg132His)	rs1441155267	0.00001
NM_030973.3(MED25):c.1482+1G>A	rs1568624159
NM_030973.4(MED25):c.1855C>A (p.Gln619Lys)	rs769034498
NM_030973.4(MED25):c.930A>T (p.Gln310His)	rs2074049426

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